{"meta":{"dataset_id":"praxikon:sys:registry:dataset:ai-act-implementation-graph","dataset_version":"2.2.0","schema_version":"1.5.0","lang":"en","effective_at":"2026-08-08T00:00:00.000Z","known_at":"2026-09-06T00:00:00.000Z","count":32,"filters":{"id":null,"type":null,"role":"authorised-representative","duty_holder":null,"topic":null},"identifiers":{"canonical_namespace":"praxikon","canonical_form":"praxikon:<jurisdiction>:<regulation>:<type>:<slug>","legacy_namespace":"raip","legacy_resolution":"permanent","resolved":{"id":null,"role":null,"duty_holder":null}}},"data":[{"id":"praxikon:eu:ai-act:action:appoint-gpai-authorised-representative","legacy_id":"raip:action:appoint-gpai-authorised-representative","type":"action","slug":"appoint-gpai-authorised-representative","version":"1.0.0","effective_at":"2025-08-02T00:00:00.000Z","known_at":"2026-08-14T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"f5a3eafa324e8ae8618656496fa8bd7c323e3a6f36d5993f3ab92493fe6d2c10","label":"Appoint an authorised representative and record the mandate","summary":"Determine whether you are the provider of the model, appoint an authorised representative established in the Union by written mandate before placing the model on the market, and write out in that mandate the four tasks in paragraph 3, the access to the Annex XI documentation and the point of contact under paragraph 4.","topics":["gpai","value-chain"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:gpai-model-provider"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":["praxikon:eu:ai-act:obligation:article-54-gpai-authorised-representative"],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[{"id":"appoint-gpai-authorised-representative-scope","operator":"all","description":"To be carried out before the model is placed on the Union market, and to be revisited on every change to the model, to the provider establishment or to the licence under which the model is released. For models placed on the market before 2 August 2025, the Article 111(3) period runs until 2 August 2027."}],"exceptions":[],"statements":[],"legal_status":"applicable","deadline_at":"2025-08-02T00:00:00.000Z","timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 54 on EUR-Lex"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"editorially_reviewed","last_checked_at":"2026-08-14T00:00:00.000Z","next_review_due_at":"2027-02-10T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:action:article-60-testing-plan-and-authorisation","legacy_id":"raip:action:article-60-testing-plan-and-authorisation","type":"action","slug":"article-60-testing-plan-and-authorisation","version":"1.0.0","effective_at":"2026-08-08T00:00:00.000Z","known_at":"2026-08-08T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"1217f5cd26f004ac01e83945ae53d4bceba7a23b98c26504248857c1446f8f04","label":"Submit the testing plan, obtain approval and register the test","summary":"Draw up a real-world testing plan, submit it to the market surveillance authority, obtain approval, register the test with a Union-wide unique single identification number, and record the division of roles with your deployer.","topics":["innovation"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:provider"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":["praxikon:eu:ai-act:obligation:article-60-real-world-testing"],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[{"id":"article-60-testing-plan-and-authorisation-scope","operator":"all","description":"Applies before you start testing in real world conditions outside a sandbox. All conditions in Article 60(4) must be met cumulatively; it is not a menu."}],"exceptions":[{"id":"article-60-testing-plan-and-authorisation-exception","operator":"not","description":"Tacit approval after 30 days applies only where national law provides for it. Where national law does not, express authorisation remains required. For the systems referred to in Annex III, points 1, 6 and 7, in law enforcement, migration, asylum and border control, registration runs through the secure non-public section of the EU database under Article 49(4), point (d). For the systems referred to in Annex III, point 2, critical infrastructure, a different route applies: Article 49(5) requires registration at national level."}],"statements":[],"legal_status":"applicable","deadline_at":"2026-08-02T00:00:00.000Z","timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 60 on EUR-Lex"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"editorially_reviewed","last_checked_at":"2026-08-08T00:00:00.000Z","next_review_due_at":"2027-02-04T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:action:article-99-101-map-penalty-tiers","legacy_id":"raip:action:article-99-101-map-penalty-tiers","type":"action","slug":"article-99-101-map-penalty-tiers","version":"1.0.0","effective_at":"2026-08-02T00:00:00.000Z","known_at":"2026-08-14T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"677f2bc0d2eedcb7da9a1b25be4939926b1fcb7cc4d93b6e0d718954a6506d58","label":"Assign to each obligation the penalty ceiling that belongs to it","summary":"Walk through your obligations register and mark per line which ceiling applies: Article 99(3) for Article 5, Article 99(4) for the role duties enumerated there, Article 25(2) and (4) and Article 50, Article 99(5) for answering information requests, and otherwise the national penalty regime under Article 99(1). Add the Article 101 regime wherever you provide a general-purpose AI model yourself, and the Article 75c regime wherever the AI Office is competent.","topics":["enforcement","governance"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:distributor","praxikon:eu:ai-act:actor:gpai-model-provider","praxikon:eu:ai-act:actor:importer","praxikon:eu:ai-act:actor:provider"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":["praxikon:eu:ai-act:obligation:article-99-101-penalties"],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[{"id":"article-99-101-map-penalty-tiers-scope","operator":"all","description":"To be done as soon as your obligations register exists, and to be revisited on every amendment of the Regulation and on every change to the national penalty regime of a Member State in which you operate. No deadline attaches to it: this is an editorial recommendation."}],"exceptions":[],"statements":[],"legal_status":"editorial","deadline_at":null,"timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 99, 100 and 101 on EUR-Lex"},{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","label":"Regulation (EU) 2026/1744, the amendment of Article 99"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"editorially_reviewed","last_checked_at":"2026-08-14T00:00:00.000Z","next_review_due_at":"2027-02-10T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:action:enter-and-maintain-eu-database-data","legacy_id":"raip:action:enter-and-maintain-eu-database-data","type":"action","slug":"enter-and-maintain-eu-database-data","version":"1.0.0","effective_at":"2026-07-27T00:00:00.000Z","known_at":"2026-08-14T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"435357e8801ee6d70b189145b8996f90aef44fa99a38559845927d9ab82c6af8","label":"Enter your data in the EU database and keep it up to date","summary":"Compile per system the data listed in Sections A and B of Annex VIII, or Section C where you are a public deployer, designate the natural person with the legal authority to register, and make sure the entry stays correct when the status, the Member States or the declaration of conformity change. Section C can only be completed after the provider has entered Section A, because point 3 asks for the URL of that entry.","topics":["conformity"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:provider","praxikon:eu:ai-act:actor:public-law-body"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":["praxikon:eu:ai-act:obligation:article-71-eu-database"],"change_ids":["praxikon:eu:ai-act:change:2026-07-27-annex-iii-date"],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[{"id":"enter-and-maintain-eu-database-data-scope","operator":"all","description":"To be carried out before the system is placed on the market, put into service or used, and again on every change that touches one of the entered fields."}],"exceptions":[],"statements":[],"legal_status":"upcoming","deadline_at":"2027-12-02T00:00:00.000Z","timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 71 on EUR-Lex"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"editorially_reviewed","last_checked_at":"2026-08-14T00:00:00.000Z","next_review_due_at":"2027-02-10T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:action:prepare-authority-information-request","legacy_id":"raip:action:prepare-authority-information-request","type":"action","slug":"prepare-authority-information-request","version":"1.0.0","effective_at":"2026-08-08T00:00:00.000Z","known_at":"2026-08-14T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"a9b903cd57dbf97bcee07bc8804068afd035cf36db986902d3479a5ac7e508f7","label":"Make your conformity file deliverable on request","summary":"Map per high-risk system where each part of the file sits, which system version it belongs to, who assembles it, how long the logs are kept and in which language indicated by the Member State concerned you can supply it, so that a reasoned request becomes a delivery task rather than a search.","topics":["high-risk-requirements"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:provider"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":["praxikon:eu:ai-act:obligation:article-21-cooperation-with-authorities"],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[{"id":"prepare-authority-information-request-scope","operator":"all","description":"To be set up before the system is placed on the market or put into service, and to be revisited on every change that produces a new system version or that alters where the logs are held. For a provider established outside the Union, the authorised representative of Article 22 belongs in the same arrangement, because the request may land with him."}],"exceptions":[],"statements":[],"legal_status":"upcoming","deadline_at":"2027-12-02T00:00:00.000Z","timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 21 on EUR-Lex"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"editorially_reviewed","last_checked_at":"2026-08-14T00:00:00.000Z","next_review_due_at":"2027-02-10T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:action:register-in-eu-database-before-market-entry","legacy_id":"raip:action:register-in-eu-database-before-market-entry","type":"action","slug":"register-in-eu-database-before-market-entry","version":"1.0.0","effective_at":"2026-08-02T00:00:00.000Z","known_at":"2026-09-06T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"21e847a8cb1d3ff7aaed32612bc5fbc191f77659dcd03cd3108289f7579b51cd","label":"Register yourself and the system before it reaches the market or is put into service","summary":"Determine per system which of the four Article 49 routes applies, the ordinary Annex III route, the Article 6(3) route, the secure section for law enforcement, migration, asylum and border control management, or the national route for point 2 of Annex III, and complete the registration before the system is placed on the market, put into service or used.","topics":["conformity","high-risk"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:distributor","praxikon:eu:ai-act:actor:provider","praxikon:eu:ai-act:actor:public-law-body"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":["praxikon:eu:ai-act:obligation:article-49-registration"],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[{"id":"register-in-eu-database-before-market-entry-scope","operator":"all","description":"Arises on every release of an Annex III system, on every application of Article 6(3) to such a system, and on every putting into service by a public authority or by a party acting on its behalf."}],"exceptions":[],"statements":[],"legal_status":"applicable","deadline_at":"2026-08-02T00:00:00.000Z","timing_basis":"text_date","high_risk_regime_from":"2027-12-02T00:00:00.000Z","links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 49 on EUR-Lex"},{"relation":"public_page","href":"/en/ai-act/artikel/49","label":"Read Article 49 in the AI Act Explorer"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"editorially_reviewed","last_checked_at":"2026-09-06T00:00:00.000Z","next_review_due_at":"2027-03-05T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:actor:authorised-representative","legacy_id":"raip:actor:authorised-representative","type":"actor","slug":"authorised-representative","version":"1.0.0","effective_at":"2026-08-08T00:00:00.000Z","known_at":"2026-08-08T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"c8f9493a2a252f9499a0a6adb239067fe4501d52259612dff91b94f3d206866c","label":"Authorised representative","summary":"The authorised representative is the party located in the Union that, on the basis of a written mandate, performs and carries out the obligations and procedures of the Regulation on behalf of a provider established outside the EU. The definition in Article 3(5) already applies today, so the role can be determined now. The appointment duty itself starts on 2 December 2027 for the standalone Annex III route and on 2 August 2028 for the embedded Annex I route. From those dates, a third-country provider may not place a high-risk AI system on the Union market without an appointed representative.","topics":["value-chain"],"actor_ids":[],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":[],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[{"id":"authorised-representative-scope","operator":"all","description":"Mandatory for providers of high-risk AI systems established in a third country, before they place those systems on the Union market (Article 22(1)). This duty starts on 2 December 2027 for the standalone Annex III route (Article 6(2)) and on 2 August 2028 for the embedded Annex I route (Article 6(1)). The definition and role determination in Article 3(5) already apply today."}],"exceptions":[{"id":"authorised-representative-exception","operator":"not","description":"Article 22 covers the high-risk AI system route. The definition in Article 3(5) also mentions general-purpose AI models; that route has its own regime, which is not elaborated here."}],"statements":[],"legal_status":"in_force","deadline_at":null,"timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 22 on EUR-Lex"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"editorially_reviewed","last_checked_at":"2026-08-08T00:00:00.000Z","next_review_due_at":"2027-02-04T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:control:article-49-pre-market-registration-gate","legacy_id":"raip:control:article-49-pre-market-registration-gate","type":"control","slug":"article-49-pre-market-registration-gate","version":"1.0.0","effective_at":"2026-08-02T00:00:00.000Z","known_at":"2026-09-06T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"c00322d9a521e62f60033115b1fdc2c26ea9847bd8687d7d0e3e1b7d3decf2c7","label":"Release gate: no market entry without registration","summary":"The control that stops any Annex III system from being placed on the market, put into service or used before the registration is complete, with an explicit check on the Article 6(3) route and on the Article 26(8) question whether the provider entry is present in the database.","topics":["conformity","control","high-risk"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:distributor","praxikon:eu:ai-act:actor:provider","praxikon:eu:ai-act:actor:public-law-body"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":["praxikon:eu:ai-act:obligation:article-49-registration"],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[],"exceptions":[],"statements":[],"legal_status":"applicable","deadline_at":"2026-08-02T00:00:00.000Z","timing_basis":"text_date","high_risk_regime_from":"2027-12-02T00:00:00.000Z","links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 49 on EUR-Lex"},{"relation":"public_page","href":"/en/ai-act/artikel/49","label":"Read Article 49 in the AI Act Explorer"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"editorially_reviewed","last_checked_at":"2026-09-06T00:00:00.000Z","next_review_due_at":"2027-03-05T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:control:article-99-101-mitigating-factor-record","legacy_id":"raip:control:article-99-101-mitigating-factor-record","type":"control","slug":"article-99-101-mitigating-factor-record","version":"1.0.0","effective_at":"2026-08-02T00:00:00.000Z","known_at":"2026-08-14T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"ecc7f911bd2521b65e45e24c8c4e5cc569b08ec97ee3cfd82a231e4acecaf993","label":"Recording of the factors in Article 99(7)","summary":"The control that ensures the factors which determine the amount of a fine are recorded at the time and not reconstructed afterwards: which technical and organisational measures were in place, when you notified an infringement yourself, how you responded to requests from the authority, and what you did to mitigate the harm suffered by affected persons. Those factors cut both ways, so the same record can also count against you; that is a reason to keep it properly rather than not at all.","topics":["control","enforcement"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:distributor","praxikon:eu:ai-act:actor:gpai-model-provider","praxikon:eu:ai-act:actor:importer","praxikon:eu:ai-act:actor:provider"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":["praxikon:eu:ai-act:obligation:article-99-101-penalties"],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[],"exceptions":[],"statements":[],"legal_status":"editorial","deadline_at":null,"timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 99, 100 and 101 on EUR-Lex"},{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","label":"Regulation (EU) 2026/1744, the amendment of Article 99"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"editorially_reviewed","last_checked_at":"2026-08-14T00:00:00.000Z","next_review_due_at":"2027-02-10T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:control:eu-database-entry-currency","legacy_id":"raip:control:eu-database-entry-currency","type":"control","slug":"eu-database-entry-currency","version":"1.0.0","effective_at":"2026-07-27T00:00:00.000Z","known_at":"2026-08-14T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"a76323e94795cd8600b3d4232a3871c6ffb670db39c3cfa01d1dc41b1000a3af","label":"Currency check on the database entry","summary":"The control that ensures a change of status, Member States, certificate or declaration of conformity leads to an updated entry within a set period, and that a public deployer notices when the provider does not enter its Section A or enters it late, instead of the public page quietly lagging behind reality.","topics":["conformity","control"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:provider","praxikon:eu:ai-act:actor:public-law-body"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":["praxikon:eu:ai-act:obligation:article-71-eu-database"],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[],"exceptions":[],"statements":[],"legal_status":"upcoming","deadline_at":"2027-12-02T00:00:00.000Z","timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 71 on EUR-Lex"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"editorially_reviewed","last_checked_at":"2026-08-14T00:00:00.000Z","next_review_due_at":"2027-02-10T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:control:gpai-mandate-review","legacy_id":"raip:control:gpai-mandate-review","type":"control","slug":"gpai-mandate-review","version":"1.0.0","effective_at":"2025-08-02T00:00:00.000Z","known_at":"2026-08-14T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"abdb7a014ca38dc4812c42694c4c21a0ae8a1ff18298f325e121fb93b02efb17","label":"Periodic review and termination of the mandate","summary":"The control that ensures the representative can actually reach the documentation, that the verification under paragraph 3(a) is repeated at a fixed moment, and that there is an agreed route for the termination under paragraph 5 with the immediate notification to the AI Office. Without such a moment a mandate stays on paper while nobody tests it.","topics":["control","gpai"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:gpai-model-provider"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":["praxikon:eu:ai-act:obligation:article-54-gpai-authorised-representative"],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[],"exceptions":[],"statements":[],"legal_status":"applicable","deadline_at":"2025-08-02T00:00:00.000Z","timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 54 on EUR-Lex"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"editorially_reviewed","last_checked_at":"2026-08-14T00:00:00.000Z","next_review_due_at":"2027-02-10T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:definition:definitie-gemachtigde","legacy_id":"raip:definition:definitie-gemachtigde","type":"definition","slug":"definitie-gemachtigde","version":"1.0.0","effective_at":"2026-08-08T00:00:00.000Z","known_at":"2026-08-08T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"1793ad1268e6a72c62e9c52cbdd27c80e19e72172e7d9ecc775c0f350e6c0d2d","label":"Authorised representative","summary":"The European point of contact for a provider from outside the Union, valid only on the basis of a written mandate.","topics":["definitions"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:gpai-model-provider","praxikon:eu:ai-act:actor:provider"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":[],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[{"id":"definitie-gemachtigde-scope","operator":"all","description":"The authorised representative is located or established in the Union and has received and accepted a written mandate."}],"exceptions":[],"statements":[{"kind":"official_fact","text":"Article 3(5) defines an authorised representative as a natural or legal person located or established in the Union who has received and accepted a written mandate from a provider of an AI system or a general-purpose AI model to, respectively, perform and carry out on its behalf the obligations and procedures established by this Regulation.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 3(5)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"editorial_interpretation","text":"The common error is that a European sales partner, reseller or subsidiary assumes it is automatically the authorised representative. That does not follow from the commercial relationship. The definition sets two cumulative requirements: the mandate is written, and it is not only given but also accepted. Without that document there is no authorised representative and the supervisory authority in the Union has no formal point of contact for that provider. A second misconception is that appointing an authorised representative transfers the provider role. It does not: the representative acts on behalf of the provider, and the provider remains the provider.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 3(5)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"recommended_action","text":"Ask every supplier from outside the Union for the name, registered address and contact details of the authorised representative and for a copy or confirmation of the accepted written mandate. Store it with the system file, because it is the first thing you need once a supervisory authority requests information about a system you source from outside the Union.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 3(5)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}}],"legal_status":"in_force","deadline_at":"2025-02-02T00:00:00.000Z","timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 3 on EUR-Lex"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"source_verified","last_checked_at":"2026-08-08T00:00:00.000Z","next_review_due_at":"2027-02-04T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:definition:definitie-operator","legacy_id":"raip:definition:definitie-operator","type":"definition","slug":"definitie-operator","version":"1.0.0","effective_at":"2026-08-08T00:00:00.000Z","known_at":"2026-08-08T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"9b6f7e5b05a7c4b4fb0ecd210e6a6d585a78ef0309b31a7358b91e81e90dcc6c","label":"Operator","summary":"The umbrella term for all six roles in the chain, and not the person operating the controls.","topics":["definitions"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:distributor","praxikon:eu:ai-act:actor:importer","praxikon:eu:ai-act:actor:provider"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":[],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[],"exceptions":[],"statements":[{"kind":"official_fact","text":"Article 3(8) defines an operator as a provider, product manufacturer, deployer, authorised representative, importer or distributor.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 3(8)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"editorial_interpretation","text":"Operator is read as the person who operates the system day to day. That is precisely what it does not mean. It is an umbrella term: where a provision addresses operators, it addresses all six listed roles at once. Anyone who skips operator obligations in a gap analysis because they believe they are only a deployer misses provisions that do apply to them. Note also that product manufacturer appears in this list as a role but is not separately defined in Article 3.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 3(8)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"recommended_action","text":"Add an operator column to your compliance overview that spells out the six roles explicitly, so that for each provision it is visible which roles are affected. Record per AI system every role your organisation holds for that specific system, because there is usually more than one.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 3(8)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}}],"legal_status":"in_force","deadline_at":"2025-02-02T00:00:00.000Z","timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 3 on EUR-Lex"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"source_verified","last_checked_at":"2026-08-08T00:00:00.000Z","next_review_due_at":"2027-02-04T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:definition:definitie-wijdverbreide-inbreuk","legacy_id":"raip:definition:definitie-wijdverbreide-inbreuk","type":"definition","slug":"definitie-wijdverbreide-inbreuk","version":"1.0.0","effective_at":"2026-08-08T00:00:00.000Z","known_at":"2026-08-08T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"bb625a0755e50f4c81ec2042b0840b7bce5cdc560ecfb5dc8348f5234e15ac05","label":"Widespread infringement","summary":"An act or omission contrary to Union law protecting the interests of individuals that harms the collective interests of persons in at least two other Member States, or that, with common features, occurs concurrently and is committed by the same operator in at least three Member States.","topics":["definitions"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:provider"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":[],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[],"exceptions":[],"statements":[{"kind":"official_fact","text":"Article 3(61) defines a widespread infringement as any act or omission contrary to Union law protecting the interest of individuals which: (a) has harmed or is likely to harm the collective interests of individuals residing in at least two Member States other than the Member State in which (i) the act or omission originated or took place, (ii) the provider concerned or, where applicable, its authorised representative is located or established, or (iii) the deployer is established, where the infringement is committed by the deployer; or (b) has caused, causes or is likely to cause harm to the collective interests of individuals and has common features, including the same unlawful practice or the same interest being infringed, and is occurring concurrently, committed by the same operator, in at least three Member States.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 3(61)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"editorial_interpretation","text":"This concept does not determine what is prohibited but how supervision is organised. Once a shortcoming in your AI system plays out the same way in several Member States, it stops being a series of separate national files and becomes one coordinated enforcement track. That is exactly the exposure of standardised software: one setting, one model or one flaw in the logic hits everywhere at once and therefore almost automatically meets the common features criterion. Note that the second limb expressly refers to the same operator, which brings deployers into scope and not only providers.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 3(61)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"recommended_action","text":"Map the Member States in which the same AI system or configuration is used and track which incidents and complaints share the same root cause across borders. Ensure that a correction made in one country is demonstrably rolled out in the others as well.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 3(61)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}}],"legal_status":"in_force","deadline_at":"2024-08-01T00:00:00.000Z","timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 3 on EUR-Lex"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"source_verified","last_checked_at":"2026-08-08T00:00:00.000Z","next_review_due_at":"2027-02-04T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:evidence:article-49-registration-dossier","legacy_id":"raip:evidence:article-49-registration-dossier","type":"evidence","slug":"article-49-registration-dossier","version":"1.0.0","effective_at":"2026-08-02T00:00:00.000Z","known_at":"2026-09-06T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"729dd580c1dc362d253e0421272c09b19c132718dd4a7135f9986f386e63b836","label":"Article 49 registration dossier","summary":"Per system: which Article 49 route was followed, the registration number, the date of registration, the name of the person who submitted it, the system version the entry relates to, and, for the secure section, a statement of which limited fields from Annex VIII and Annex IX were completed.","topics":["conformity","evidence","high-risk"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:distributor","praxikon:eu:ai-act:actor:provider","praxikon:eu:ai-act:actor:public-law-body"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":["praxikon:eu:ai-act:obligation:article-49-registration"],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[],"exceptions":[],"statements":[],"legal_status":"applicable","deadline_at":"2026-08-02T00:00:00.000Z","timing_basis":"text_date","high_risk_regime_from":"2027-12-02T00:00:00.000Z","links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 49 on EUR-Lex"},{"relation":"public_page","href":"/en/ai-act/artikel/49","label":"Read Article 49 in the AI Act Explorer"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"editorially_reviewed","last_checked_at":"2026-09-06T00:00:00.000Z","next_review_due_at":"2027-03-05T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:evidence:article-99-101-penalty-exposure-register","legacy_id":"raip:evidence:article-99-101-penalty-exposure-register","type":"evidence","slug":"article-99-101-penalty-exposure-register","version":"1.0.0","effective_at":"2026-08-02T00:00:00.000Z","known_at":"2026-08-14T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"26861e8785e9779404427f4167ee17b0f32121936562af6e3e6c27102fa2060a","label":"Register of penalty ceilings per obligation","summary":"Per obligation: which ceiling attaches to it and on which provision that rests, whether the level follows from national law and if so from which, and whether the Article 101 or Article 75c regime is added on top. This is the document that shows a board there is no single amount, and that substantiates where you make your controls heavier.","topics":["enforcement","evidence"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:distributor","praxikon:eu:ai-act:actor:gpai-model-provider","praxikon:eu:ai-act:actor:importer","praxikon:eu:ai-act:actor:provider"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":["praxikon:eu:ai-act:obligation:article-99-101-penalties"],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[],"exceptions":[],"statements":[],"legal_status":"editorial","deadline_at":null,"timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 99, 100 and 101 on EUR-Lex"},{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","label":"Regulation (EU) 2026/1744, the amendment of Article 99"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"editorially_reviewed","last_checked_at":"2026-08-14T00:00:00.000Z","next_review_due_at":"2027-02-10T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:evidence:eu-database-entry-record","legacy_id":"raip:evidence:eu-database-entry-record","type":"evidence","slug":"eu-database-entry-record","version":"1.0.0","effective_at":"2026-07-27T00:00:00.000Z","known_at":"2026-08-14T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"747c0a6a89a43d904575e42fa3906bb5d79d282308d08ef4c0eb964f4fe4a5a0","label":"EU database registration file","summary":"Per system: which Annex VIII data was entered, by which natural person with the legal authority to do so, on what date, in which version, when the entry was last checked against reality, and for a public deployer the URL of the entry made by the provider. This is also the file that shows the public entry and your internal documents say the same thing.","topics":["conformity","evidence"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:provider","praxikon:eu:ai-act:actor:public-law-body"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":["praxikon:eu:ai-act:obligation:article-71-eu-database"],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[],"exceptions":[],"statements":[],"legal_status":"upcoming","deadline_at":"2027-12-02T00:00:00.000Z","timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 71 on EUR-Lex"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"editorially_reviewed","last_checked_at":"2026-08-14T00:00:00.000Z","next_review_due_at":"2027-02-10T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:evidence:gpai-representative-mandate-file","legacy_id":"raip:evidence:gpai-representative-mandate-file","type":"evidence","slug":"gpai-representative-mandate-file","version":"1.0.0","effective_at":"2025-08-02T00:00:00.000Z","known_at":"2026-08-14T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"c48344fa977400be55c1d5713e695114d36fd9a1af8343301b43ea121cd8eb7b","label":"Mandate file of the authorised representative","summary":"The written mandate itself, in an official language of the institutions of the Union, together with the copy of the Annex XI technical documentation, the contact details of the provider, and the record of the verification under paragraph 3(a). The provider grants the mandate and supplies the documentation; the ten year retention after the placing on the market rests under paragraph 3(b) with the representative, which keeps the file at the disposal of the AI Office and national competent authorities.","topics":["evidence","gpai"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:gpai-model-provider"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":["praxikon:eu:ai-act:obligation:article-54-gpai-authorised-representative"],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[],"exceptions":[],"statements":[],"legal_status":"applicable","deadline_at":"2025-08-02T00:00:00.000Z","timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 54 on EUR-Lex"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"editorially_reviewed","last_checked_at":"2026-08-14T00:00:00.000Z","next_review_due_at":"2027-02-10T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:obligation:article-111-legacy-public-systems","legacy_id":"raip:obligation:article-111-legacy-public-systems","type":"obligation","slug":"article-111-legacy-public-systems","version":"1.0.0","effective_at":"2026-07-27T00:00:00.000Z","known_at":"2026-08-14T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"f6d9b4b81b0a9ef37eec8fdd812d98a712cc1688491f8db5c61b8a857ee419e4","label":"Article 111(2): legacy high-risk systems and the 2 August 2030 date","summary":"High-risk AI systems placed on the market or put into service before the date of application of Chapter III, since the Digital Omnibus 2 December 2027 for Annex III systems and 2 August 2028 for Annex I systems, come under the high-risk requirements of that Chapter only once their design is significantly changed as from that date. This is not an exemption from the whole Regulation: Article 4 and Article 50 keep running. For systems intended to be used by public authorities the carve out falls away entirely: their providers and deployers must in any case comply with the requirements and obligations by 2 August 2030.","topics":["high-risk","timeline"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:distributor","praxikon:eu:ai-act:actor:importer","praxikon:eu:ai-act:actor:provider"],"duty_holder_ids":["praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:provider"],"affected_actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:distributor","praxikon:eu:ai-act:actor:importer"],"oversight_actor_ids":[],"evidence_owner_ids":["praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:provider"],"duty_holder_uncertainty_status":null,"interpretation_status":"preliminary","interpretation_note":"The text above is the consolidated text and has been checked against the Official Journal; what is preliminary is our reading of it. First, the cut off date. The amended paragraph 2 refers not to a date but to the date of application of Chapter III referred to in Article 113, and since the Digital Omnibus Article 113, third paragraph, point (c) gives two: 2 December 2027 for Annex III and 2 August 2028 for Annex I. We therefore read the cut off as route dependent. A defensible alternative reading is that the reference points at the general application date of Chapter III as a whole, that is 2 August 2026, because Sections 4 and 5 of that Chapter were not deferred; on that reading the cut off would effectively still be 2 August 2026. We follow the route dependent reading because point (c) expressly names Sections 1, 2 and 3, and those are the Sections carrying the requirements the grace period exists for. Second, the notion of a significant change in the design. That is not the same wording as the defined substantial modification used elsewhere in the Regulation, and there is no guidance or case law saying whether a model update, a retraining run or a new data source counts. We read it as a change that touches the intended purpose, the functioning or the risk profile, and not as every release. Third, the reach of intended to be used by public authorities. It is unclear whether a system supplied to both public and private customers falls under it in full, and whether a private party carrying out a public task is a public authority. We read the intention as following from the market the system is offered for and not from the legal form of the individual customer.","obligation_ids":[],"change_ids":["praxikon:eu:ai-act:change:2026-07-27-annex-iii-date","praxikon:eu:ai-act:change:2026-12-02-article-50-marking-grace-ends","praxikon:eu:ai-act:change:2028-08-02-annex-i-high-risk-applicable"],"action_ids":["praxikon:eu:ai-act:action:assess-significant-design-change","praxikon:eu:ai-act:action:plan-legacy-public-system-compliance"],"evidence_ids":["praxikon:eu:ai-act:evidence:legacy-system-transition-register"],"control_ids":["praxikon:eu:ai-act:control:design-change-review-gate"],"template_ids":["praxikon:eu:ai-act:template:article-111-legal-text"],"conditions":[{"id":"article-111-2-scope-article-5-unaffected","operator":"all","description":"The transitional rule is without prejudice to the application of Article 5, as referred to in Article 113, third paragraph, point (a). A prohibited practice remains prohibited, regardless of when the system was placed on the market or put into service and regardless of whether the design has changed."},{"id":"article-111-2-scope-limited-to-chapter-iii","operator":"all","description":"The transitional rule concerns the high-risk requirements of Chapter III and is not an exemption from the whole Regulation. Article 4 has applied since 2 February 2025 irrespective of when a system reached the market, and Article 50 has applied to all systems in scope since 2 August 2026. The paragraph 4 added by the Digital Omnibus confirms this: it gives legacy generative systems a short extra period for Article 50(2), which would make no sense if Article 50 did not reach them."},{"id":"article-111-2-legacy-scope","operator":"all","description":"Applies to operators of high-risk AI systems placed on the market or put into service before the date of application of Chapter III referred to in Article 113, other than the systems referred to in paragraph 1 that are components of the large-scale IT systems listed in Annex X. That date is 2 December 2027 for systems that are high-risk under Article 6(2) and Annex III, and 2 August 2028 for systems that are high-risk under Article 6(1) and Annex I. For that group the high-risk requirements bite only once the systems are subject to significant changes in their designs as from that date."},{"id":"article-111-2-type-and-model","operator":"all","description":"The grace period runs per type and model, not per unit. If at least one individual unit of the type and model was lawfully placed on the market or put into service before the cut off date, other units of the same type and model are covered too and may be offered without additional obligations, requirements or additional certification, as long as the design remains unchanged. The decisive date is the one on which the first unit of that type and model was placed on the market or put into service in the Union."},{"id":"article-111-2-public-authority-deadline","operator":"all","description":"Applies independently to providers and deployers of high-risk AI systems intended to be used by public authorities. They must in any case take the necessary steps to comply with the requirements and obligations of the Regulation by 2 August 2030, even where the design remains unchanged."}],"exceptions":[{"id":"article-111-2-exception-annex-x-systems","operator":"not","description":"Systems that are components of the large-scale IT systems established by the legal acts listed in Annex X fall not under paragraph 2 but under paragraph 1. Paragraph 1 was not amended by the Digital Omnibus and keeps its own cut off: placed on the market or put into service before 2 August 2027, with compliance by 31 December 2030."}],"statements":[{"kind":"official_fact","text":"Without prejudice to the application of Article 5 as referred to in Article 113, third paragraph, point (a), this Regulation shall apply to operators of high-risk AI systems, other than the systems referred to in paragraph 1 of this Article, that have been placed on the market or put into service before the date of application of Chapter III referred to in Article 113, only if, as from that date, those systems are subject to significant changes in their designs. In any case, the providers and deployers of high-risk AI systems intended to be used by public authorities shall take the necessary steps to comply with the requirements and obligations laid down in this Regulation by 2 August 2030.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Amended Article 111(2)","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"Chapter III, Sections 1, 2 and 3, with the exception of Article 6(5), applies from 2 December 2027 as regards AI systems classified as high-risk pursuant to Article 6(2) and Annex III, and from 2 August 2028 as regards AI systems classified as high-risk pursuant to Article 6(1) and Annex I.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Amended Article 113 application dates","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"Providers of AI systems, including general-purpose AI systems, generating synthetic audio, image, video or text content, that have been placed on the market before 2 August 2026 shall take the necessary steps in order to comply with Article 50(2) by 2 December 2026.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"New Article 111(4)","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"The grace period in paragraph 2 applies where the type and model of an AI system has already been placed on the market. If at least one individual unit was lawfully placed on the market or put into service before the cut off date, the grace period also covers other units of the same type and model, which may be offered without additional obligations, requirements or mandatory additional certification, as long as the design remains unchanged. On a significant change to the design after the cut off date the provider must fully comply with all relevant provisions applicable to high-risk AI systems, including the conformity assessment requirements.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Recital 39 of Regulation (EU) 2026/1744","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"editorial_interpretation","text":"In practice this provision is read exactly the wrong way round. Executives hear that existing systems are left alone and conclude that nothing is needed until well into the 2030s. That is wrong in two ways. For a public sector organisation the second sentence gives no escape but a deadline, and it applies whether or not you change anything about the system. And for everyone the transitional rule concerns only the high-risk requirements: Article 4 has been running since February 2025 and Article 50 since August 2026, with legacy generative systems having only until 2 December 2026 to get the machine-readable marking of Article 50(2) in order. The first sentence, moreover, is not a resting place but a switch. As soon as the design is significantly changed you must comply fully with what applies to high-risk systems, the conformity assessment first of all; those duties do follow the shifted calendar of 2 December 2027 and 2 August 2028. That switching moment rarely arises at a time you choose: it arises on a supplier update, a migration or a new data source. Two things therefore matter more than the date itself. You need to know when the first unit of each type and model reached the market, because that is the decisive date and without it you cannot later show which track a system was on. And you need a moment in your change process at which someone assesses whether a change is significant, before it goes live.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Amended Article 111(2)","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Recital 39 of Regulation (EU) 2026/1744","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"New Article 111(4)","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"recommended_action","text":"Determine per type and model of your high-risk AI systems when the first unit was placed on the market or put into service, and whether the system is intended to be used by public authorities. Record that determination with a date and a reasoning, and note which route applies, because that decides whether your cut off is 2 December 2027 or 2 August 2028. For the systems intended for public authority use, set a plan towards 2 August 2030 that counts back from the conformity assessment and the registration, not from the end date. Also build into your change and release process a review moment at which someone records whether an intended design change is significant, before the change goes into production. Separately, check whether Article 111(4) catches you: if so you have until 2 December 2026 for the marking under Article 50(2).","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Amended Article 111(2)","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Amended Article 113 application dates","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"New Article 111(4)","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}}],"legal_status":"applicable","deadline_at":"2030-08-02T00:00:00.000Z","timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"public_page","href":"https://www.praxikon.com/en/verplichtingen/article-111-legacy-public-systems","label":"Open the human explanation"},{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Regulation (EU) 2024/1689 on EUR-Lex"},{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","label":"Regulation (EU) 2026/1744 on EUR-Lex, which amends Article 111"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"source_verified","last_checked_at":"2026-08-14T00:00:00.000Z","next_review_due_at":"2027-02-10T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:obligation:article-18-document-retention","legacy_id":"raip:obligation:article-18-document-retention","type":"obligation","slug":"article-18-document-retention","version":"1.0.0","effective_at":"2026-07-27T00:00:00.000Z","known_at":"2026-08-14T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"0971f35c7a7daaf1306f4fbd7ae98680b8b1e2da44b5a84a5abf7d7610cbdbfb","label":"Article 18: documentation keeping","summary":"The provider of a high-risk AI system keeps the technical documentation, the quality management system documentation, the changes approved by notified bodies and the decisions they issued, and the EU declaration of conformity at the disposal of the national competent authorities for a period ending ten years after the system has been placed on the market or put into service.","topics":["high-risk-requirements"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:provider"],"duty_holder_ids":["praxikon:eu:ai-act:actor:provider"],"affected_actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer"],"oversight_actor_ids":[],"evidence_owner_ids":["praxikon:eu:ai-act:actor:provider"],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":[],"change_ids":[],"action_ids":["praxikon:eu:ai-act:action:keep-high-risk-documentation-available"],"evidence_ids":["praxikon:eu:ai-act:evidence:article-18-retention-dossier"],"control_ids":["praxikon:eu:ai-act:control:article-18-retention-review"],"template_ids":["praxikon:eu:ai-act:template:article-18-legal-text"],"conditions":[{"id":"article-18-scope","operator":"all","description":"Applies to the provider of a high-risk AI system. The period ends ten years after the system has been placed on the market or put into service."},{"id":"article-18-financial-institutions-regime","operator":"all","description":"Where the provider is a financial institution subject to requirements regarding internal governance, arrangements or processes under Union financial services law, it maintains the technical documentation of point (a) as part of the documentation it already keeps under that law. That is not an exemption from the retention duty but an indication of the regime in which it is carried out for that one component. Paragraph 3 does not mention points (b) to (e)."}],"exceptions":[],"statements":[{"kind":"official_fact","text":"Paragraph 1 provides that the provider shall, for a period ending 10 years after the high-risk AI system has been placed on the market or put into service, keep at the disposal of the national competent authorities: (a) the technical documentation referred to in Article 11; (b) the documentation concerning the quality management system referred to in Article 17; (c) the documentation concerning the changes approved by notified bodies, where applicable; (d) the decisions and other documents issued by the notified bodies, where applicable; (e) the EU declaration of conformity referred to in Article 47. Paragraph 2 provides that each Member State shall determine conditions under which that documentation remains at the disposal of the national competent authorities for the period indicated for the cases when a provider or its authorised representative established on its territory goes bankrupt or ceases its activity prior to the end of that period. Paragraph 3 provides that providers that are financial institutions subject to requirements regarding their internal governance, arrangements or processes under Union financial services law shall maintain the technical documentation as part of the documentation kept under the relevant Union financial services law.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 18(1)-(3)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"The amended application dates for Chapter III, Sections 1, 2 and 3, with the exception of Article 6(5), are 2 December 2027 for the standalone Annex III route and 2 August 2028 for high-risk AI in products covered by the Annex I harmonisation legislation.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Amended Article 113 application dates","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"editorial_interpretation","text":"Four things here are our reading and not the text. First the application date: Regulation (EU) 2026/1744 does not name Article 18 separately, so the fact that this duty moves with 2 December 2027 and 2 August 2028 follows from its placement in Chapter III, Section 3, and not from an explicit provision. Second the starting moment. Paragraph 1 names the placing on the market and the putting into service side by side without choosing, and for a system where both moments occur that is years of difference at the end of the period. Counting from the later moment is the only count that falls short under neither reading, and that is what we would advise a provider. The other reading is defensible: in Union product law the placing on the market is usually the moment that counts, and then the period ends earlier. Third a substantially modified version: the text is silent, and it is equally defensible that every version gets its own period as that the original one continues. Fourth the reach of paragraph 3: it names only the technical documentation, so we keep points (b) to (e) under the general regime until the contrary is settled. Paragraph 2, finally, is addressed to the Member State and not to you. The Netherlands has not yet determined those conditions, so what happens to your file on insolvency or cessation of activity currently follows from contract and not from law.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 18(1)-(3)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"editorial_interpretation","text":"Watch the boundaries of this duty, because they get crossed in both directions. The automatically generated logs are not among the five components: they fall under Article 19, with its own and much shorter period of at least six months, appropriate to the intended purpose, and with a clause for financial institutions that parallels paragraph 3. So do not stretch the ten years to your logs, and conversely do not settle for six months for your documentation. For a provider established in a third country the actual availability moreover sits with two parties at once: Article 22(3)(b) requires the authorised representative to keep, for ten years, the contact details of the provider, a copy of the EU declaration of conformity, the technical documentation and, if applicable, the certificate issued by the notified body at the disposal of the competent authorities and of the bodies referred to in Article 74(10). Two files that drift apart are worse than one. Point (e) overlaps with Article 47(1), which gives the declaration of conformity its own ten year period, and under Article 23(5) the importer carries ten years again for the certificate, the instructions for use and the declaration of conformity. That overlap is no reason to drop one of the periods: they are independent duties of different parties. It is a reason to choose a place of retention where they coincide. On the GDPR, finally: a retention duty under Union law is itself a ground under Article 6(1)(c) GDPR, and the storage limitation of Article 5(1)(e) permits retention that the law requires. The question is therefore not whether it is allowed but how far it reaches. Ten years applies to what Article 18(1) names, and not to everything created along the way: separate test sets, log samples and raw data dumps from the documentation you must be able to produce.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 18(1)-(3)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"editorial_interpretation","text":"This is the duty that asks nothing at the moment you take it on and everything at the moment you have forgotten it. Ten years is longer than the average life of a supplier contract, a document management system and a product team. In the organisations where we encounter this, the five components rarely sit in one archive: the quality system sits with compliance, the notified body decisions with certification, the declaration of conformity with legal. That is not law, but it is common enough that it is worth checking before you assume your situation is different. Whoever first assembles the documents when an authority asks discovers that retention in fact depended on a person and not on a process. Note also the side that is not about you: paragraph 2 concerns the situation where the provider or its representative goes bankrupt, and that is exactly the risk you run as a customer of a small supplier. It is a contracting question before it becomes a compliance question.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 18(1)-(3)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"recommended_action","text":"Designate per high-risk system one place of retention where the five components of paragraph 1 come together. Record side by side when the system was placed on the market and when it was put into service, and calculate the end date from the later of those two moments, so that you do not fall short under either reading. Set that end date as a commitment in a system that survives a change of staff, and keep the Article 19 logs separately with their own period. If you work with an authorised representative, record who holds which copy, because Article 22(3)(b) places the same availability on them as well. When procuring a high-risk system, put in the contract what happens to the documentation if the supplier stops or goes bankrupt, because paragraph 2 leaves that arrangement to national law that does not yet exist in the Netherlands.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 18(1)-(3)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}}],"legal_status":"upcoming","deadline_at":"2027-12-02T00:00:00.000Z","timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"public_page","href":"https://www.praxikon.com/en/verplichtingen/article-18-document-retention","label":"Open the human explanation"},{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 18 on EUR-Lex"},{"relation":"public_page","href":"/en/ai-act/artikel/18","label":"Read Article 18 in the AI Act Explorer"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"source_verified","last_checked_at":"2026-08-14T00:00:00.000Z","next_review_due_at":"2027-02-10T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:obligation:article-20-corrective-actions","legacy_id":"raip:obligation:article-20-corrective-actions","type":"obligation","slug":"article-20-corrective-actions","version":"1.0.0","effective_at":"2026-08-08T00:00:00.000Z","known_at":"2026-08-14T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"3da4413e7f76d6cd26cf52cc894dc8b6637916ab4ed1d39776d4446a96c5232c","label":"Article 20: corrective actions and duty of information","summary":"A provider that considers, or has reason to consider, that a high-risk AI system it has placed on the market or put into service is not in conformity with the Regulation must immediately take the necessary corrective actions and inform the distributors accordingly, and, where applicable, also the deployers, the authorised representative and the importers. Where that system also presents a risk within the meaning of Article 79(1), the provider must immediately investigate the causes and inform the competent market surveillance authorities and, where applicable, the notified body that issued a certificate under Article 44.","topics":["high-risk-requirements","post-market"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:distributor","praxikon:eu:ai-act:actor:importer","praxikon:eu:ai-act:actor:provider"],"duty_holder_ids":["praxikon:eu:ai-act:actor:provider"],"affected_actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:distributor","praxikon:eu:ai-act:actor:importer"],"oversight_actor_ids":["praxikon:eu:ai-act:actor:market-surveillance-authority"],"evidence_owner_ids":["praxikon:eu:ai-act:actor:provider"],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":[],"change_ids":[],"action_ids":["praxikon:eu:ai-act:action:run-corrective-action-procedure"],"evidence_ids":["praxikon:eu:ai-act:evidence:corrective-action-record"],"control_ids":["praxikon:eu:ai-act:control:non-conformity-escalation-gate"],"template_ids":["praxikon:eu:ai-act:template:article-20-legal-text"],"conditions":[{"id":"article-20-scope","operator":"all","description":"Applies to providers of high-risk AI systems as soon as they consider, or have reason to consider, that a system they have placed on the market or put into service is not in conformity with this Regulation. For the standalone Annex III route (Article 6(2)) the date is 2 December 2027. For systems embedded as a safety component in products covered by the Annex I harmonisation legislation (Article 6(1)) the date is 2 August 2028."},{"id":"article-20-risk-trigger","operator":"any","description":"The second layer in paragraph 2 is added only where the system presents a risk within the meaning of Article 79(1) and the provider becomes aware of that risk. The investigation of causes and the duty to inform the market surveillance authorities and, where applicable, the notified body that issued a certificate under Article 44, then come on top of the corrective actions under paragraph 1."},{"id":"article-20-article-25-1-becoming-provider","operator":"any","description":"The distributor, the importer and the deployer appear here as affected parties, but that is not their only possible position. Anyone who puts their name or trade mark on a high-risk system already placed on the market, who substantially modifies such a system, or who changes the intended purpose of a system not classified as high-risk so that it becomes high-risk, is considered a provider under Article 25(1) and is subject to the obligations of Article 16. Point (j) of that Article routes straight to Article 20, so this provision then becomes a duty of their own rather than a notification arriving from someone else. In the trade mark case this applies without prejudice to contractual arrangements allocating the obligations otherwise."}],"exceptions":[{"id":"article-20-legacy-systems-article-111-2","operator":"not","description":"Article 20 is by definition about systems already placed on the market or put into service, and that is exactly the group covered by the transitional rule of Article 111(2). That provision was replaced by Article 1, point (39)(a), of Regulation (EU) 2026/1744 and now reads: without prejudice to the application of Article 5 as referred to in Article 113, third paragraph, point (a), this Regulation applies to operators of high-risk AI systems, other than the systems referred to in paragraph 1 of that Article, that have been placed on the market or put into service before the date of application of Chapter III referred to in Article 113, only if, as from that date, those systems are subject to significant changes in their designs. The cut-off is therefore no longer a fixed date in paragraph 2: the date of 2 August 2026 that stood there until that amendment has been removed, and the amended paragraph names no date of its own. The carve-out in paragraph 1 covers systems that are components of the large-scale IT systems listed in Annex X; paragraph 1 was not amended and keeps a cut-off of its own. For systems intended to be used by public authorities the reprieve in paragraph 2 does not hold: there, compliance with the requirements and obligations is due by 2 August 2030 in any event. Which date of application of Chapter III is the cut-off is an open point: the object on Article 111 reads it as route dependent, so 2 December 2027 for the Annex III route and 2 August 2028 for the Annex I route, and marks that reading expressly as preliminary. That question is carried there, not here."}],"statements":[{"kind":"official_fact","text":"Paragraph 1. Providers of high-risk AI systems which consider or have reason to consider that a high-risk AI system that they have placed on the market or put into service is not in conformity with this Regulation shall immediately take the necessary corrective actions to bring that system into conformity, to withdraw it, to disable it, or to recall it, as appropriate. They shall inform the distributors of the high-risk AI system concerned and, where applicable, the deployers, the authorised representative and importers accordingly. Paragraph 2. Where the high-risk AI system presents a risk within the meaning of Article 79(1) and the provider becomes aware of that risk, it shall immediately investigate the causes, in collaboration with the reporting deployer, where applicable, and inform the market surveillance authorities competent for the high-risk AI system concerned and, where applicable, the notified body that issued a certificate for that high-risk AI system in accordance with Article 44, in particular, of the nature of the non-compliance and of any relevant corrective action taken.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 20(1)-(2)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"For the Annex III route this requirement applies from 2 December 2027; for high-risk AI in regulated products (Annex I) from 2 August 2028.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Article 1, point (40)(b), of Regulation (EU) 2026/1744, replacing Article 113, third paragraph, point (c), of Regulation (EU) 2024/1689","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"editorial_interpretation","text":"This provision is rarely read as a procedure, and that is exactly where it goes wrong. Article 20 places four measures side by side that differ sharply in practice, and those four are not legally equivalent. Recall and withdrawal are defined in Article 3(16) and (17), and the knowledge base carries those terms separately; the difference between them is the point in the chain. Bringing a system into conformity is the patch. Disabling is the odd one out: it is practically the heaviest switch, because it stops a customer who is running the system, and it is at the same time the only one of the four the Regulation nowhere defines. Anyone who copies that word into a contract or procedure without deciding for themselves what it means leaves the heaviest measure the vaguest. The second half is the notification, and in practice that is what fails most often. Paragraph 1 asks you to reach your distributors and, where applicable, your deployers, authorised representatives and importers, which is only possible if you hold a current list of who runs the system in which version and through which contact you reach them. That list is not a by-product of your CRM: resale, white labelling and integration mean you have customers you do not know.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 20(1)-(2)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"editorial_interpretation","text":"Paragraph 2 and Article 73 are often built as a single reporting channel, and that goes wrong in two ways. The trigger differs: Article 73 concerns a serious incident that has occurred, Article 20(2) a risk within the meaning of Article 79(1), that is, a risk to the health, safety or fundamental rights of persons. That is not a tidy split between past and future: a serious incident that has occurred usually also means the system presents a risk, so in practice both provisions often fire at the same time. Nor do the recipients differ entirely, because both routes run to market surveillance authorities. The difference sits in the detail: Article 73(1) points to the authorities of the Member States where the incident occurred, Article 20(2) to the authorities competent for the system concerned, and only Article 20(2) adds the notified body that issued a certificate under Article 44. Only Article 73, moreover, sets hard deadlines. So build one internal process with two exits, not two separate channels and not one channel that forgets the notified body.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 20(2), Article 73(1)-(2) and Article 79(1)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"editorial_interpretation","text":"Two things within this duty are unsettled. First, what \"immediately\" requires: Article 20 sets no period. The closest anchor in the Regulation is Article 73(2), which ties \"immediately\" to the moment the provider has established a causal link between the system and the incident, or the reasonable likelihood of such a link, with an outer limit of fifteen days after becoming aware. We read Article 20 in that light: act once the signal is confirmed, and not only after a full internal investigation has been completed, because paragraph 2 places the investigation of causes alongside the measures rather than before them. A defensible alternative reading is that a provider first has reasonable time to verify and that \"immediately\" only starts running once the non-conformity is established. Second, the threshold \"reason to consider\": it is nowhere settled whether a complaint from a deployer, a deviating test result or a signal from the post-market monitoring of Article 72 already meets it. Whoever records that themselves can later demonstrate the moment of becoming aware; whoever does not has to reconstruct it after the fact.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 20(2), Article 73(1)-(2) and Article 79(1)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"recommended_action","text":"Write out the four measures in paragraph 1 as four concrete scenarios with an owner, a decision maker and a lead time, and decide for yourself what disabling means in your system, because the Regulation does not define that term. Test at least once whether you can actually disable or recall a system without needing a fresh decision to do so. Also keep a record, per system version, of who runs it and through which contact you reach that party, and record which signal meets the \"reason to consider\" threshold in your organisation, so that the moment of becoming aware is demonstrable rather than something reconstructed after the fact.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 20(1)-(2)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}}],"legal_status":"upcoming","deadline_at":"2027-12-02T00:00:00.000Z","timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"public_page","href":"https://www.praxikon.com/en/verplichtingen/article-20-corrective-actions","label":"Open the human explanation"},{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 20 on EUR-Lex"},{"relation":"related","href":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","label":"Binding amended application calendar"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"source_verified","last_checked_at":"2026-08-14T00:00:00.000Z","next_review_due_at":"2027-02-10T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:obligation:article-21-cooperation-with-authorities","legacy_id":"raip:obligation:article-21-cooperation-with-authorities","type":"obligation","slug":"article-21-cooperation-with-authorities","version":"1.0.0","effective_at":"2026-08-08T00:00:00.000Z","known_at":"2026-08-14T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"559250092044f24993e3f2608cae8b25215c5e18ff58592e1379c9eb746c62a3","label":"Article 21: cooperation with competent authorities","summary":"Upon a reasoned request by a competent authority, the provider of a high-risk AI system provides all the information and documentation necessary to demonstrate conformity with the requirements of Chapter III, Section 2, in a language which can be easily understood by the authority in one of the official languages of the institutions of the Union as indicated by the Member State concerned. Upon the same request the provider also gives, as applicable, access to the automatically generated logs, to the extent those logs are under its control.","topics":["high-risk-requirements"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:provider"],"duty_holder_ids":["praxikon:eu:ai-act:actor:provider"],"affected_actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer"],"oversight_actor_ids":[],"evidence_owner_ids":["praxikon:eu:ai-act:actor:provider"],"duty_holder_uncertainty_status":null,"interpretation_status":"preliminary","interpretation_note":"Two things are unsettled here, and the status carries a cost that we state alongside them. First, who the competent authority is. Article 21 refers without qualification to a competent authority. Article 3(48) defines the national competent authority as a notifying authority or a market surveillance authority, and provides in the same point that, as regards AI systems put into service or used by Union institutions, agencies, offices and bodies, references to national competent authorities or market surveillance authorities are construed as references to the European Data Protection Supervisor. We read Article 21 as addressing those national competent authorities. The stronger alternative reading is that competence follows Chapter IX: the market surveillance authority designated by the Member State, the financial supervisor via Article 74(6), the data protection supervisory authority via Article 74(8), the European Data Protection Supervisor via Article 74(9), and, for a delimited group of systems, the AI Office via Article 75 as amended by Regulation (EU) 2026/1744, which already applies. On that reading you prepare for a different counterpart than the one we assume here. Second, what paragraph 2 asks when the logs are in fact held by the deployer. The text limits the duty to logs under your control but does not say whether you must arrange access contractually in order to retain that control. We read no separate duty into it; that is our reading and not the text. What is settled here is the date of application, and that corrects an earlier reading of ours. Article 1, point (40)(b), of Regulation (EU) 2026/1744 replaces Article 113, third paragraph, point (c), and expressly sets Chapter III, Sections 1, 2 and 3, with the exception of Article 6(5), at 2 December 2027 for systems classified as high-risk pursuant to Article 6(2) and Annex III and at 2 August 2028 for those classified as high-risk pursuant to Article 6(1) and Annex I. Article 21 sits in Section 3 and is therefore covered by that provision in so many words; the fact that the omnibus does not name Article 21 individually changes nothing, because the provision operates per Section. The cost of this status: a preliminary reading does not count in the per-situation derivation of obligations, so the log access of paragraph 2 and the language rule do not surface there, and Article 16(k) covers only the demonstration of conformity. The object stays reachable through its own page, the deadline index and the API.","obligation_ids":[],"change_ids":[],"action_ids":["praxikon:eu:ai-act:action:prepare-authority-information-request"],"evidence_ids":["praxikon:eu:ai-act:evidence:authority-request-response-file"],"control_ids":["praxikon:eu:ai-act:control:authority-request-intake-and-deadline"],"template_ids":["praxikon:eu:ai-act:template:article-21-legal-text"],"conditions":[{"id":"article-21-scope","operator":"all","description":"Applies to providers of high-risk AI systems as soon as a competent authority makes a reasoned request. For the standalone Annex III route (Article 6(2)) the date is 2 December 2027. For systems that are high-risk under Article 6(1) and relate to products covered by Annex I, Section A, the date is 2 August 2028. For products covered by Annex I, Section B, Article 21 does not apply at all: amended Article 2(2) makes only Article 6(1), Article 60a and Articles 102 to 112 applicable there, and Article 21 is not on that list. That is not a corner case, because the Machinery Regulation (EU) 2023/1230 has been moved from Section A to Section B. Note also the new Article 2(13): for systems under Annex I, Section A, the Commission may limit the application of Articles 17 to 25, and therefore of Article 21, by delegated act."},{"id":"article-21-legacy-systems","operator":"any","description":"For systems already running, the amended Article 111(2) applies: without prejudice to the application of Article 5 as referred to in Article 113, third paragraph, point (a), the Regulation applies to operators of high-risk AI systems, other than those referred to in Article 111(1), placed on the market or put into service before the date of application of Chapter III referred to in Article 113, only if, as from that date, those systems are subject to significant changes in their designs. The reference date is therefore no longer 2 August 2026 but whichever date applies to the system: 2 December 2027 for the Annex III route and 2 August 2028 for the Annex I route. For systems intended to be used by public authorities the date of 2 August 2030 applies in any case."},{"id":"article-21-confidentiality-treatment","operator":"all","description":"What the authority obtains pursuant to this Article is treated in accordance with the confidentiality obligations of Article 78. That is not a limit on the duty to supply and therefore not an exception: it is how what you supplied is handled on the receiving side."}],"exceptions":[{"id":"article-21-log-access-limits","operator":"not","description":"Paragraph 2 carries two limits, not one. Access to the automatically generated logs applies \"as applicable\", and it applies \"to the extent such logs are under their control\". Logs held solely by the deployer therefore fall outside what the provider can supply under this Article; the deployer keeps those logs itself under Article 26(6)."}],"statements":[{"kind":"official_fact","text":"Paragraph 1 provides that providers of high-risk AI systems shall, upon a reasoned request by a competent authority, provide that authority all the information and documentation necessary to demonstrate the conformity of the high-risk AI system with the requirements set out in Section 2, in a language which can be easily understood by the authority in one of the official languages of the institutions of the Union as indicated by the Member State concerned. Paragraph 2 provides that, upon a reasoned request by a competent authority, providers shall also give the requesting competent authority, as applicable, access to the automatically generated logs of the high-risk AI system referred to in Article 12(1), to the extent such logs are under their control. Paragraph 3 provides that any information obtained by a competent authority pursuant to this Article shall be treated in accordance with the confidentiality obligations set out in Article 78.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 21(1)-(3)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-14T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"The surroundings of Article 21, verbatim. Article 22(3), point (c), requires the authorised representative to provide a competent authority, upon a reasoned request, with all the information and documentation necessary to demonstrate conformity with the requirements set out in Section 2, including access to the logs referred to in Article 12(1) to the extent such logs are under the control of the provider; the final subparagraph of that paragraph provides that the mandate shall empower the authorised representative to be addressed, in addition to or instead of the provider, by the competent authorities. Article 19(1) provides that the provider keeps the logs under its control for a period appropriate to the intended purpose, of at least six months. Article 26(6) imposes the same period of at least six months on the deployer for the logs under its control. Article 99(5) subjects the supply of incorrect, incomplete or misleading information to notified bodies or national competent authorities in reply to a request to administrative fines of up to EUR 7 500 000 or, if the offender is an undertaking, up to 1 % of total worldwide annual turnover for the preceding financial year, whichever is higher.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 12(1); Article 19(1); Article 21(1)-(3); Article 22(3); Article 26(6); Article 74(1); Article 78; Article 99(5)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-14T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"The surroundings as Regulation (EU) 2026/1744 left them. Article 1, point (34), amends Article 77. The heading now reads \"Powers of authorities protecting fundamental rights and cooperation with market surveillance authorities\". Paragraph 1 now provides that national public authorities or bodies which supervise or enforce the respect of obligations under Union law protecting fundamental rights, including the right to non-discrimination, have the power to request and access any information or documentation created or maintained pursuant to this Regulation from the relevant market surveillance authority, in accessible language and machine-readable format by electronic means, where access to that information or documentation is necessary for effectively fulfilling their mandates within the limits of their jurisdiction, and that the Article is without prejudice to the competences, tasks, powers and independence of those authorities or bodies. The restriction to the systems listed in Annex III, the requirement of an accessible format and the after-the-fact notification of the market surveillance authority are gone. Inserted paragraph 1a provides that the market surveillance authority grants that access, including by requesting the information or documentation from the provider or the deployer where necessary and without undue delay. Inserted paragraph 1b requires market surveillance authorities and those authorities or bodies to cooperate closely and to provide each other with mutual assistance, including exchange of information. Article 99(4) still does not list Article 21 after the amendment: Article 1, point (38)(b), only inserts a point (da) there on the obligations of providers and operators pursuant to Article 25(2) and (4).","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Article 1, point (34), amending Article 77; Article 1, point (38)(b), inserting point (da) into Article 99(4)","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"}],"review":{"reviewed_at":"2026-08-14T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"The timeline this object rests on is stated in so many words in the amended Regulation. Article 1, point (40)(b), replaces Article 113, third paragraph, point (c), so that Chapter III, Sections 1, 2 and 3, with the exception of Article 6(5), applies from 2 December 2027 as regards AI systems classified as high-risk pursuant to Article 6(2) and Annex III, and from 2 August 2028 as regards AI systems classified as high-risk pursuant to Article 6(1) and Annex I. Article 1, point (39)(a), replaces Article 111(2), so that the grace period is tied to the date of application of Chapter III referred to in Article 113 and no longer to 2 August 2026, while retaining 2 August 2030 for systems intended to be used by public authorities. Article 1, point (2)(a), replaces Article 2(2), so that for systems classified as high-risk under Article 6(1) related to products covered by Annex I, Section B, only Article 6(1), Article 60a and Articles 102 to 112 apply; Article 21 is not on that list. Article 1, point (41), deletes point 1 of Annex I, Section A, and adds Regulation (EU) 2023/1230 on machinery to Annex I, Section B.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Article 1, point (40)(b), replacing Article 113, third paragraph, point (c)","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Article 1, point (39)(a), replacing Article 111(2)","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Article 1, point (2)(a), replacing Article 2(2); Article 1, point (41), amending Annex I","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"}],"review":{"reviewed_at":"2026-08-14T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"editorial_interpretation","text":"Most of what is requested here already exists under the Regulation: the technical documentation of Article 11, the logs of Articles 12 and 19, the quality management system of Article 17, the conformity file of Article 43. Two things are genuinely additional. Article 19 requires you to keep the logs; Article 21(2) requires you to give an authority access to them, which is a different act. And the language rule of paragraph 1 is additional, because you deliver in an official language of the institutions of the Union chosen by the Member State concerned, not in the language you find most convenient. There is nothing to agree there; find out which language the Member State concerned has indicated and budget translation capacity for a technical file. Three further things go wrong in practice. Your documentation exists but is spread across teams and systems, so assembling it takes weeks. Your documentation belongs to a different system version than the one the question is about, in which case you demonstrate the conformity of something else. And the logs are gone: Article 19(1) and Article 26(6) ask for at least six months, so a request arriving later can meet an empty drawer. A provider established in a third country should also expect the request to land with its authorised representative: Article 22(3), point (c), imposes nearly the same delivery on him and the mandate empowers him to be addressed in addition to or instead of the provider. Article 21 is not the only channel either, but that second channel now runs differently. Under amended Article 77(1) a fundamental rights body requests information or documentation from the relevant market surveillance authority rather than directly from you, in accessible language and machine-readable format, and the restriction to Annex III systems has gone. Under inserted paragraph 1a that market surveillance authority may then request the material from you or from the deployer without undue delay. So expect a fundamental rights question to reach you as a request from the market surveillance authority, in a format a machine can read, and with its own route to testing under Article 77(3). On paragraph 3, finally, no comfortable story: Article 78 protects what you hand over only in accordance with Union or national law, carves out the cases of Article 5 of Directive (EU) 2016/943 for trade secrets and source code, and in paragraph 4 leaves the exchange of information, the dissemination of warnings and information duties under national criminal law unaffected. It is a rule on handling, not a shield.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 12(1); Article 19(1); Article 21(1)-(3); Article 22(3); Article 26(6); Article 74(1); Article 78; Article 99(5)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Article 1, point (34), amending Article 77; Article 1, point (38)(b), inserting point (da) into Article 99(4)","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"recommended_action","text":"Treat this as a delivery exercise rather than a documentation question. Record per high-risk system where each part of the conformity file sits, which system version it belongs to and who can assemble it within an agreed period. Find out which official language of the institutions of the Union the Member State concerned has indicated, and plan translation capacity instead of a language agreement. Determine per customer contract whether the automatically generated logs are under your control or with the deployer, and check that your retention period reaches the six months of Article 19(1), because otherwise the question can no longer be answered after half a year. If you are established outside the Union, record that your authorised representative can deliver the same file, since under Article 22(3), point (c), he is addressed in addition to or instead of you. And let nobody improvise in the answer: supplying incorrect, incomplete or misleading information in reply to a request is a separate ground for a fine under Article 99(5), in a different band from the obligations that Article 99(4) does list.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 12(1); Article 19(1); Article 21(1)-(3); Article 22(3); Article 26(6); Article 74(1); Article 78; Article 99(5)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Article 1, point (34), amending Article 77; Article 1, point (38)(b), inserting point (da) into Article 99(4)","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}}],"legal_status":"upcoming","deadline_at":"2027-12-02T00:00:00.000Z","timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"public_page","href":"https://www.praxikon.com/en/verplichtingen/article-21-cooperation-with-authorities","label":"Open the human explanation"},{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 21 on EUR-Lex"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"source_verified","last_checked_at":"2026-08-14T00:00:00.000Z","next_review_due_at":"2027-02-10T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:obligation:article-49-registration","legacy_id":"raip:obligation:article-49-registration","type":"obligation","slug":"article-49-registration","version":"1.0.0","effective_at":"2026-08-02T00:00:00.000Z","known_at":"2026-09-06T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"95cd9f806f657817dbdc6e5aa1c1b74b37239b8513edc6ad054fd87eaf7b858f","label":"Article 49: registration in the EU database before the system reaches the market","summary":"The provider of a high-risk AI system listed in Annex III, or where applicable its authorised representative, registers itself and that system in the EU database before it is placed on the market or put into service. The same duty applies to the provider that concludes under Article 6(3) that its Annex III system is precisely not high-risk: that provider too registers itself and that system. The deployer that is a public authority or a Union body, or that acts on behalf of such an authority, registers itself, selects the system and registers its use. For the areas of law enforcement, migration, asylum and border control management the registration goes into a secure non-public section with fewer fields, to which only the Commission and the national authorities referred to in Article 74(8) have access. For the systems in point 2 of Annex III registration does not run through the EU database but at national level.","topics":["conformity","high-risk"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:distributor","praxikon:eu:ai-act:actor:provider","praxikon:eu:ai-act:actor:public-law-body"],"duty_holder_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:provider","praxikon:eu:ai-act:actor:public-law-body"],"affected_actor_ids":["praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:distributor"],"oversight_actor_ids":["praxikon:eu:ai-act:actor:market-surveillance-authority"],"evidence_owner_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:provider","praxikon:eu:ai-act:actor:public-law-body"],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":[],"change_ids":[],"action_ids":["praxikon:eu:ai-act:action:register-in-eu-database-before-market-entry"],"evidence_ids":["praxikon:eu:ai-act:evidence:article-49-registration-dossier"],"control_ids":["praxikon:eu:ai-act:control:article-49-pre-market-registration-gate"],"template_ids":["praxikon:eu:ai-act:template:article-49-legal-text"],"conditions":[{"id":"article-49-route-secure-section","operator":"any","description":"Paragraph 4 does not except the registration but relocates it: for the systems referred to in points 1, 6 and 7 of Annex III in the areas of law enforcement, migration, asylum and border control management, the registration referred to in paragraphs 1, 2 and 3 goes into a secure non-public section of the EU database, with a limited list of fields from Annex VIII and Annex IX, and only the Commission and the national authorities referred to in Article 74(8) have access to it."},{"id":"article-49-scope-provider","operator":"any","description":"Applies where a provider or, where applicable, an authorised representative places on the market or puts into service a high-risk AI system listed in Annex III, and where that same party places on the market or puts into service an AI system for which it has concluded that it is not high-risk according to Article 6(3)."},{"id":"article-49-scope-public-deployer","operator":"any","description":"Applies where a deployer that is a public authority, Union institution, body, office or agency, or a person acting on their behalf, puts into service or uses a high-risk AI system listed in Annex III."},{"id":"article-49-timing","operator":"all","description":"Registration is a precondition and not a notification afterwards: paragraphs 1 and 2 attach to the moment before the system is placed on the market or put into service, paragraph 3 to the moment before it is put into service or used."}],"exceptions":[{"id":"article-49-exception-annex-iii-point-2","operator":"not","description":"This is an exception to the route and not to the duty. Paragraphs 1 and 3 except the high-risk AI systems referred to in point 2 of Annex III from registration in the EU database, and paragraph 5 provides that those systems are registered at national level. For critical infrastructure the registration therefore does not fall away: it runs through the national register rather than through the Article 71 EU database."}],"statements":[{"kind":"editorial_interpretation","text":"Two readings existed of the date on this object, and Chef chose between them on 6 September 2026. Article 49 sits in Section 5 of Chapter III, and the third paragraph of Article 113 names a Section of Chapter III twice: point (b) names Section 4 and sets it at 2 August 2025, and point (c) names Sections 1, 2 and 3, with the exception of Article 6(5). Section 5 appears in neither point, nor in point (a) or point (d). Article 49 therefore falls under the general date in the second paragraph, and that is the date this object carries: 2 August 2026. Whoever places an Annex III system on the market today without registering is late, not early. The practical reading is not written away but sits alongside it: the duty only acquires an object once a high-risk AI system exists, and that status arises through Article 6(2) and Annex III on 2 December 2027, the date named in point (c) of the third paragraph as replaced by Article 1, point (40)(b), of Regulation (EU) 2026/1744. That date sits in high_risk_regime_from and the ground of the chosen date in timing_basis. The decision is recorded in data/ai-act/review/decision-d1-application-dates.json.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 49(1)-(5)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Article 1, point (40)(b), replacing Article 113, third paragraph, point (c)","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"official_fact","text":"Paragraph 1 provides that, before placing on the market or putting into service a high-risk AI system listed in Annex III, with the exception of high-risk AI systems referred to in point 2 of Annex III, the provider or, where applicable, the authorised representative shall register themselves and their system in the EU database referred to in Article 71. Paragraph 2 provides that, before placing on the market or putting into service an AI system for which the provider has concluded that it is not high-risk according to Article 6(3), that provider or, where applicable, the authorised representative shall register themselves and that system in the EU database referred to in Article 71. Paragraph 3 provides that, before putting into service or using a high-risk AI system listed in Annex III, with the exception of high-risk AI systems listed in point 2 of Annex III, deployers that are public authorities, Union institutions, bodies, offices or agencies or persons acting on their behalf shall register themselves, select the system and register its use in the EU database referred to in Article 71.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 49(1)-(5)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"Paragraph 4 provides that, for high-risk AI systems referred to in points 1, 6 and 7 of Annex III, in the areas of law enforcement, migration, asylum and border control management, the registration referred to in paragraphs 1, 2 and 3 of this Article shall be in a secure non-public section of the EU database referred to in Article 71 and shall include only the following information, as applicable, referred to in: (a) Section A, points 1 to 10, of Annex VIII, with the exception of points 6, 8 and 9; (b) Section B, points 1 to 5, and points 8 and 9 of Annex VIII; (c) Section C, points 1 to 3, of Annex VIII; (d) points 1, 2, 3 and 5, of Annex IX. Only the Commission and national authorities referred to in Article 74(8) shall have access to the respective restricted sections of the EU database listed in the first subparagraph of this paragraph. Paragraph 5 provides that high-risk AI systems referred to in point 2 of Annex III shall be registered at national level.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 49(1)-(5)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"editorial_interpretation","text":"Paragraph 2 is the most expensive sentence in this article and it is missed systematically. Anyone invoking the Article 6(3) exception for an Annex III system believes they have stepped out of the high-risk regime. That is true for the requirements on the system, but not for the registration: it is precisely that provider that registers itself and that system in the EU database, and does so before it is placed on the market or put into service. The exception is therefore not free. It is paid for in visibility: your name, your system and the Article 6(3) condition you rely on end up in a publicly searchable register, exactly where you thought you would stay out of sight. The mistake that follows is predictable and expensive. An organisation carries out the Article 6(3) assessment properly, documents it, and skips the registration because in its mind that belongs to the high-risk regime. The result is that the database holds no trace of a choice it did in fact make deliberately, and that a regulator meets it as a party that simply failed to register the system. The matching piece of evidence already exists in this knowledge base as the registration record for the Article 6(3) route and hangs off the Annex III obligation; the object below covers registration under paragraphs 1, 3, 4 and 5. Note the sequence, finally. Registration is a precondition, not a notification afterwards. Delivering first and registering later repairs nothing: the moment the duty is breached is the placing on the market itself.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 49(1)-(5)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 6(2)-(4), Article 49 and Annex III","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"editorial_interpretation","text":"Read Article 49 together with Article 71 and with Article 26(8), because those three form a chain that in practice stalls at its weakest point. Article 71 describes the database and says who fills in which fields; Article 49 says when that must happen and by whom; Article 26(8) turns the result into a procurement condition. That last one is the sharpest: a deployer with the status of a public authority that establishes that the system it intends to use is not registered in the EU database shall not use that system and shall inform the provider or the distributor. For a supplier that means a missing registration is not an administrative backlog but a block on the public market, and the party raising it with you is your own customer. For a public sector organisation it means the check belongs in the procurement process and not at the moment of deployment. Two routes deviate and are forgotten for exactly that reason. The first is paragraph 4: for the areas of law enforcement, migration, asylum and border control management the registration moves into a secure non-public section with a shorter list of fields, and only the Commission and the national authorities referred to in Article 74(8) can look into it. That is not an exemption but a different counter, and whoever reads it as an exemption registers nothing. The second is paragraph 5: the systems in point 2 of Annex III, critical infrastructure, are registered at national level. The Regulation does not say which national register that is, so you answer that question in national law and not here. For a grid operator or a water utility that is the difference between an existing counter and a search that only starts once the system is already running.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 49(1)-(5)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 26(1)-(12)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"recommended_action","text":"Make registration a hard gate in the release process, before the moment of placing on the market or putting into service, not after. Work through three questions per system. First: does the intended purpose fall under a point of Annex III, and if so, under which point. Second: are you relying on Article 6(3). If you are, the registration in paragraph 2 is your duty and not your choice, and you register yourself and that system, together with the condition you rely on. Third: if it concerns point 2 of Annex III, the registration does not go to the EU database but to national level, and you locate that counter before you need the system. If you are a public sector organisation, do not only register yourself but also select the system and register its use, and build the Article 26(8) check into your procurement process: no deployment as long as the provider entry is not in the database, with a written notification to the provider or the distributor where it is missing. If you supply into the areas of law enforcement, migration, asylum or border control management, record that your registration runs through the secure non-public section and which limited fields go into it. Keep, per system, the registration number, the date of registration and the name of the person who submitted it, together with the system version the entry relates to, and update that entry as soon as the intended purpose, the status or the conformity documentation changes.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 49(1)-(5)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 26(1)-(12)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}}],"legal_status":"applicable","deadline_at":"2026-08-02T00:00:00.000Z","timing_basis":"text_date","high_risk_regime_from":"2027-12-02T00:00:00.000Z","links":[{"relation":"public_page","href":"https://www.praxikon.com/en/verplichtingen/article-49-registration","label":"Open the human explanation"},{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 49 on EUR-Lex"},{"relation":"public_page","href":"/en/ai-act/artikel/49","label":"Read Article 49 in the AI Act Explorer"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"source_verified","last_checked_at":"2026-09-06T00:00:00.000Z","next_review_due_at":"2027-03-05T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:obligation:article-54-gpai-authorised-representative","legacy_id":"raip:obligation:article-54-gpai-authorised-representative","type":"obligation","slug":"article-54-gpai-authorised-representative","version":"1.0.0","effective_at":"2025-08-02T00:00:00.000Z","known_at":"2026-08-14T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"0c470c29e8f0c2ad222dc0517b6a9437615474bfc6429e9c37b90eb35572d5c5","label":"Article 54: authorised representative of a provider of a GPAI model","summary":"A provider established in a third country appoints, by written mandate, an authorised representative established in the Union before placing a general-purpose AI model on the Union market. The representative performs the tasks the mandate assigns to it and provides a copy of that mandate to the AI Office upon request. The mandate empowers it at least to verify the documentation, keep a copy available for ten years, provide information and cooperate, and appoints it as the point of contact in addition to or instead of the provider.","topics":["gpai","value-chain"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:gpai-model-provider"],"duty_holder_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:gpai-model-provider"],"affected_actor_ids":[],"oversight_actor_ids":["praxikon:eu:ai-act:actor:ai-office"],"evidence_owner_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:gpai-model-provider"],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":["praxikon:eu:ai-act:obligation:article-53-gpai","praxikon:eu:ai-act:obligation:article-55-gpai-systemic-risk"],"change_ids":[],"action_ids":["praxikon:eu:ai-act:action:appoint-gpai-authorised-representative"],"evidence_ids":["praxikon:eu:ai-act:evidence:gpai-representative-mandate-file"],"control_ids":["praxikon:eu:ai-act:control:gpai-mandate-review"],"template_ids":["praxikon:eu:ai-act:template:article-54-legal-text"],"conditions":[{"id":"article-54-scope","operator":"all","description":"Applies where the model qualifies as a general-purpose AI model within the meaning of Article 3(63), its provider is established in a third country, and that model is placed on the Union market. The appointment is made by written mandate within the meaning of Article 3(5), which is not only given but also accepted, and it is made before the model is placed on the market. The moment at which the latter occurs is fixed less sharply for a model than for a system; see the editorial interpretation."},{"id":"article-54-market-date-transition","operator":"any","description":"For models placed on the market from 2 August 2025, the appointment duty applies from that moment. Providers of models placed on the market before 2 August 2025 shall, under Article 111(3), take the necessary steps to comply with the obligations of the Regulation by 2 August 2027."}],"exceptions":[{"id":"article-54-open-source-exception","operator":"not","description":"Paragraph 6 excludes the obligation for providers of AI models released under a free and open-source licence that allows access, usage, modification and distribution, and whose parameters, including the weights, the information on the model architecture and the information on model usage, are made publicly available. That exception falls away as soon as the model presents a systemic risk. Whether a given release qualifies is a factual test that has not been settled anywhere; we read it narrowly, so a partially public release does not qualify."}],"statements":[{"kind":"official_fact","text":"Paragraph 1 provides that, prior to placing a general-purpose AI model on the Union market, providers established in third countries shall, by written mandate, appoint an authorised representative which is established in the Union. Paragraph 2 provides that the provider shall enable its authorised representative to perform the tasks specified in the mandate received from the provider. Paragraph 3 provides that the authorised representative shall perform the tasks specified in the mandate received from the provider, that it shall provide a copy of the mandate to the AI Office upon request in one of the official languages of the institutions of the Union, and that for the purposes of the Regulation the mandate shall empower the authorised representative to carry out the following tasks: (a) verify that the technical documentation specified in Annex XI has been drawn up and all obligations referred to in Article 53 and, where applicable, Article 55 have been fulfilled by the provider; (b) keep a copy of the technical documentation specified in Annex XI at the disposal of the AI Office and national competent authorities, for a period of 10 years after the general-purpose AI model has been placed on the market, and the contact details of the provider that appointed the authorised representative; (c) provide the AI Office, upon a reasoned request, with all the information and documentation, including that referred to in point (b), necessary to demonstrate compliance with the obligations in that Chapter; (d) cooperate with the AI Office and competent authorities, upon a reasoned request, in any action they take in relation to the general-purpose AI model, including when the model is integrated into AI systems placed on the market or put into service in the Union. Paragraph 4 provides that the mandate shall empower the authorised representative to be addressed, in addition to or instead of the provider, by the AI Office or the competent authorities, on all issues related to ensuring compliance with the Regulation. Paragraph 5 provides that the authorised representative shall terminate the mandate if it considers or has reason to consider the provider to be acting contrary to its obligations pursuant to the Regulation, and that in such a case it shall also immediately inform the AI Office about the termination of the mandate and the reasons therefor. Paragraph 6 provides that the obligation set out in that Article shall not apply to providers of general-purpose AI models that are released under a free and open-source licence that allows for the access, usage, modification, and distribution of the model, and whose parameters, including the weights, the information on the model architecture, and the information on model usage, are made publicly available, unless the general-purpose AI models present systemic risks.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 54(1)-(6)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 3(5)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"Article 113(3)(b) provides that Chapter III Section 4, Chapter V, Chapter VII and Chapter XII and Article 78 shall apply from 2 August 2025, with the exception of Article 101. Article 54 sits in Chapter V and therefore applies from 2 August 2025.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 113(3)(b)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"Article 101(1) provides that the Commission may impose on providers of general-purpose AI models fines not exceeding 3 percent of their annual total worldwide turnover in the preceding financial year or EUR 15 000 000, whichever is higher. Article 101 is excluded by Article 113(3)(b) from the earlier application of Chapter XII and has therefore applied since 2 August 2026. The obligation in Article 54 has thus applied since 2 August 2025, while the Commission fining power behind it exists only since 2 August 2026.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 101(1)-(6)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 113(3)(b)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"Providers of general-purpose AI models that have been placed on the market before 2 August 2025 shall take the necessary steps in order to comply with the obligations laid down in the Regulation by 2 August 2027.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 111(3)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"editorial_interpretation","text":"This article touches two parties that rarely see themselves that way. The first is the model provider outside the Union that assumes nothing is required until a European customer asks: paragraph 1 places the appointment before the placing on the market, so the representative should exist before the first user in the Union can access the model. The second is the European party that accepts the mandate. It is not stepping into a mailbox role, but note how paragraph 3 is built: the first sentence obliges it to perform the tasks the mandate assigns to it, and only then does the article list what the mandate empowers it to do. Points (a) to (d) are therefore mandate content and empowerment, and its duty runs through them. That is where this article leaves its sharpest question open: is a representative that accepts a mandate omitting task (a) or (b) itself in breach, or does the failure rest entirely with the provider that drew up the mandate. We read paragraph 3 as making the list mandatory minimum content, so that a mandate lacking it does not satisfy the article, which leaves the provider answerable under paragraph 1 and the representative answerable for what it did accept. A defensible alternative reading is that a representative signing without those powers takes on a task it cannot discharge and thereby falls short itself. So do not assume the ten year retention in point (b) rests on you automatically, or automatically does not; write it out. Paragraph 5 closes this off in a way that is often missed: a representative that considers, or has reason to consider, that the provider is breaching its obligations terminates the mandate and immediately informs the AI Office. That is a duty rather than a power, and it calls for access to the documentation agreed in advance and for a moment at which that access is tested.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 54(1)-(6)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"editorial_interpretation","text":"Three things about the timeline and the scope. First, the difference between duty and enforcement: the duty has applied since 2 August 2025, but Article 101 is excluded from the earlier application, so the Commission can only fine since 2 August 2026. For a provider outside the Union discovering today that it has no representative, that means: in breach for well over a year, and now also exposed to a fine. Second, the relationship with Article 22. That article carries the same figure for high-risk AI systems, starting on 2 December 2027 and 2 August 2028; Article 54 is the separate route for general-purpose AI models and has applied since 2 August 2025. Anyone looking up the role of authorised representative finds both and needs to know which route applies. Third, the trigger in paragraph 1. The Regulation fixes the moment of placing on the market less sharply for a model than for a system, and for a model made available only through an interface from a third country there is no case law. We read the duty as starting once the model is made available to users in the Union in the course of a commercial activity, because paragraph 1 attaches to placing on the market and not to establishment in the Union. A defensible alternative reading is that making a model available through an interface is not placing the model itself on the market, so that the duty only arises on an actual supply of the model.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 54(1)-(6)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 113(3)(b)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Article 1, point (40)(b) and (c), replacing Article 113, third paragraph, point (c) and adding point (d)","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"recommended_action","text":"First establish whether you are the provider of the model or only a user, because only the provider appoints. If you are established outside the Union, put the mandate in writing before the model becomes available here, and write the four tasks in paragraph 3 into it expressly, together with the access to the Annex XI documentation and the point of contact under paragraph 4. If your model was already on the market before 2 August 2025, work to 2 August 2027 rather than to today. If you are only now discovering that there is no representative, assume the duty has run since 2 August 2025 and that the Commission has been able to fine since 2 August 2026; remedy first and record when you did. If you accept a mandate, agree in advance how you carry out the verification in paragraph 3(a), who holds the copy for ten years, and at what moment you test whether termination under paragraph 5 is called for.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 54(1)-(6)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 101(1)-(6)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}}],"legal_status":"applicable","deadline_at":"2025-08-02T00:00:00.000Z","timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"public_page","href":"https://www.praxikon.com/en/verplichtingen/article-54-gpai-authorised-representative","label":"Open the human explanation"},{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 54 on EUR-Lex"},{"relation":"public_page","href":"/en/ai-act/artikel/54","label":"Read Article 54 in the AI Act Explorer"},{"relation":"related","href":"/en/ai-act/artikel/53","label":"Article 53: the duties the representative verifies"},{"relation":"related","href":"https://digital-strategy.ec.europa.eu/en/policies/guidelines-gpai-providers","label":"Guidelines for GPAI model providers"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"source_verified","last_checked_at":"2026-08-14T00:00:00.000Z","next_review_due_at":"2027-02-10T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:obligation:article-71-eu-database","legacy_id":"raip:obligation:article-71-eu-database","type":"obligation","slug":"article-71-eu-database","version":"1.0.0","effective_at":"2026-07-27T00:00:00.000Z","known_at":"2026-08-14T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"ceaa3da5b4cb893e068c9cbe5094b7934da65e8a20cc7cf57546945c0b877c06","label":"Article 71: EU database for high-risk AI systems listed in Annex III","summary":"The provider or, where applicable, the authorised representative enters the data listed in Sections A and B of Annex VIII into the EU database; the deployer who is, or who acts on behalf of, a public authority, agency or body enters the data listed in Section C. Information registered in accordance with Article 49 is publicly available in a user-friendly manner and machine-readable, except for the secure section covering law enforcement, migration, asylum and border control management and the registration of testing in real world conditions. Setting up and maintaining the database itself is a task of the Commission and not a duty of yours.","topics":["conformity","high-risk"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:provider","praxikon:eu:ai-act:actor:public-law-body"],"duty_holder_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:provider","praxikon:eu:ai-act:actor:public-law-body"],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:provider","praxikon:eu:ai-act:actor:public-law-body"],"duty_holder_uncertainty_status":null,"interpretation_status":"preliminary","interpretation_note":"Two things about the law itself are unsettled here. First, the date. Article 71 falls under the general application date of 2 August 2026, while the entry duties in paragraphs 2 and 3 hang on the registration in Article 49, whose Annex III route was shifted to 2 December 2027 by Regulation (EU) 2026/1744. We therefore read the practical deadline as 2 December 2027. Two alternative readings are defensible, and they point in opposite directions: the mild one is that the database exists from 2 August 2026 and only the entering follows the later date, so whoever registers earlier is not being early but on time; the hard one is that the amended Article 113, third paragraph, point (c), names only Chapter III, Sections 1, 2 and 3, while Article 49 sits in Section 5 of that same Chapter, so the registration duty may not have moved with it and you may already be late rather than early. Anyone planning against this deadline is planning against our reading and not against a settled fact. Second, the Article 60 route. Article 60 sits in Chapter VI and the provider or prospective provider testing in real world conditions today must register under Article 60(4), point (c), in accordance with Article 71(4). Whether that route moved with the Annex III deferral or already runs under the general date of 2 August 2026 is unsettled. The fact that 2026/1744 widened the scope of Article 60 to Annex I Section A and placed an Article 60a alongside it for Annex I Section B makes that question larger rather than smaller. This object does not carry that duty and the status here says nothing about it. Settled, and therefore no longer a ground for the preliminary status: the content of Section B of Annex VIII. Article 1, point (42), of Regulation (EU) 2026/1744 deletes points 7 and 9, and the reading above follows that text rather than the base regulation. One cross-reference does follow from it that the legislator did not chase down: Article 49(4) is unamended and still lists point 9 of Section B for the secure section, a point that no longer exists. Whoever works through that list literally is looking for a field that is not there. In addition, and this expressly does not carry the status because it is not an unsettled reading but a coverage gap of this dataset: paragraphs 1 and 6 address the Commission, which is not an actor here, so this object carries only the entry duties of paragraphs 2 and 3; and paragraph 3 also names whoever acts on behalf of a public authority, a role that does not exist separately alongside the body governed by public law, so a private party registering on behalf of a public authority has to assess for itself whether paragraph 3 rests on it.","obligation_ids":[],"change_ids":["praxikon:eu:ai-act:change:2026-07-27-annex-iii-date"],"action_ids":["praxikon:eu:ai-act:action:enter-and-maintain-eu-database-data"],"evidence_ids":["praxikon:eu:ai-act:evidence:eu-database-entry-record"],"control_ids":["praxikon:eu:ai-act:control:eu-database-entry-currency"],"template_ids":["praxikon:eu:ai-act:template:article-71-legal-text"],"conditions":[{"id":"article-71-scope","operator":"any","description":"Applies where a provider or authorised representative places an Annex III high-risk AI system on the market or puts it into service and registers itself and that system in accordance with Article 49, where that same party registers a system considered not to be high-risk pursuant to Article 6(3), or where a deployer that is, or that acts on behalf of, a public authority, agency or body registers itself, selects the system and registers its use."}],"exceptions":[{"id":"article-71-exception-annex-iii-point-2","operator":"not","description":"Article 49(5) provides that high-risk AI systems referred to in point 2 of Annex III are registered at national level. For those systems the registration therefore does not run through the Article 71 EU database."},{"id":"article-71-exception-secure-section","operator":"not","description":"Paragraph 4 excludes the section referred to in Article 49(4) from public availability. For the systems referred to in points 1, 6 and 7 of Annex III in the areas of law enforcement, migration, asylum and border control management, registration takes place in a secure non-public section of the database, with fewer fields than the full Sections: Section A, points 1 to 10 with the exception of points 6, 8 and 9; Section B, points 1 to 5 and points 8 and 9; Section C, points 1, 2 and 3; and points 1, 2, 3 and 5 of Annex IX. Only the Commission and the national authorities referred to in Article 74(8) have access to those sections. Mind the cross-reference: Article 49(4) was not amended by Regulation (EU) 2026/1744 and therefore still names point 9 of Section B, while Article 1, point (42), of that same Regulation deleted that point. There is nothing left to fill in there."},{"id":"article-71-exception-real-world-testing","operator":"not","description":"Paragraph 4 additionally excludes the section referred to in Article 60(4), point (c). The main rule there is not a secure section: the provider or prospective provider registers the testing in real world conditions in accordance with Article 71(4), with a Union wide unique single identification number and the information specified in Annex IX. Under the third sentence of paragraph 4 that information is accessible only to market surveillance authorities and the Commission, unless the provider or prospective provider has given consent for also making it accessible to the public. Only for points 1, 6 and 7 of Annex III does the testing registration go into the secure non-public section under Article 49(4), point (d), and for point 2 of Annex III to national level under Article 49(5)."}],"statements":[{"kind":"official_fact","text":"Paragraph 1 provides that the Commission shall, in collaboration with the Member States, set up and maintain an EU database containing the information referred to in paragraphs 2 and 3 concerning high-risk AI systems referred to in Article 6(2) which are registered in accordance with Articles 49 and 60, and AI systems that are not considered as high-risk pursuant to Article 6(3) and which are registered in accordance with Article 6(4) and Article 49. When setting the functional specifications the Commission shall consult the relevant experts, and when updating them the Board. Paragraph 2 provides that the data listed in Sections A and B of Annex VIII shall be entered into the database by the provider or, where applicable, by the authorised representative. Paragraph 3 provides that the data listed in Section C of Annex VIII shall be entered by the deployer who is, or who acts on behalf of, a public authority, agency or body, in accordance with Article 49(3) and (4). Paragraph 4 provides that, with the exception of the section referred to in Article 49(4) and Article 60(4), point (c), the information registered in accordance with Article 49 shall be accessible and publicly available in a user-friendly manner, and that the information should be easily navigable and machine-readable. The same paragraph provides that the information registered in accordance with Article 60 shall be accessible only to market surveillance authorities and the Commission, unless the prospective provider or provider has given consent for also making the information accessible to the public. Paragraph 5 provides that the database shall contain personal data only in so far as necessary for collecting and processing information in accordance with this Regulation, and that such information shall include the names and contact details of natural persons who are responsible for registering the system and have the legal authority to represent the provider or the deployer. Paragraph 6 provides that the Commission shall be the controller of the database, shall make adequate technical and administrative support available to providers, prospective providers and deployers, and that the database shall comply with the applicable accessibility requirements.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 71(1)-(6)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"Annex VIII sets out which information is submitted upon registration and kept up to date thereafter. Section A, for providers registering in accordance with Article 49(1), lists thirteen points, including the name, address and contact details of the provider and of the authorised representative, the trade name and any additional unambiguous reference allowing identification and traceability of the system, a description of the intended purpose and of the components and functions supported, a basic and concise description of the information used and of the operating logic, the status of the system, the details and a scanned copy of the notified body certificate where applicable, the Member States where the system is available, a copy of the EU declaration of conformity referred to in Article 47 and the electronic instructions for use, which are not provided for the law enforcement, migration, asylum and border control management areas of points 1, 6 and 7 of Annex III. Section C, for deployers registering under Article 49(3), lists five points: the name, address and contact details of the deployer, the same details of the person submitting information on its behalf, the URL of the entry of the system in the database by its provider, a summary of the findings of the fundamental rights impact assessment carried out in accordance with Article 27, and where applicable a summary of the data protection impact assessment. Neither Section was amended by Regulation (EU) 2026/1744.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Annex VIII, Sections A and C","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"Section B of Annex VIII, for registrations under Article 49(2), was amended. Article 1, point (42), of Regulation (EU) 2026/1744 reads: \"in Annex VIII, section B, points 7 and 9 are deleted\". Deleted are therefore point 7, the short summary of the grounds on which the AI system is considered not to be high-risk in application of the procedure under Article 6(3), and point 9, the statement of any Member States in which the system has been placed on the market, put into service or made available in the Union. The Regulation does not renumber the remaining points. Section B therefore now lists seven points, numbered 1 to 6 and 8: the name, address and contact details of the provider; the same details of another person submitting information on the provider behalf; the same details of the authorised representative where applicable; the trade name and any additional unambiguous reference allowing identification and traceability of the system; a description of the intended purpose; the condition or conditions under Article 6(3) on the basis of which the system is considered not to be high-risk; and the status of the system. Recital 22 of 2026/1744 explains that registration is thereby made simpler and more proportionate, while expressly maintaining that a provider applying Article 6(3) remains obliged to document its assessment before the system is placed on the market or put into service, and that national competent authorities may request that assessment.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Annex VIII, Section B","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Article 1, point (42), deleting Annex VIII, Section B, points 7 and 9","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Recital 22 of Regulation (EU) 2026/1744","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"Article 49(4) lists exhaustively what goes into the secure non-public section, and that is less than the full Sections: Section A, points 1 to 10 with the exception of points 6, 8 and 9; Section B, points 1 to 5 and points 8 and 9; Section C, points 1, 2 and 3; and points 1, 2, 3 and 5 of Annex IX. The final subparagraph provides that only the Commission and the national authorities referred to in Article 74(8) have access to the respective restricted sections of the database. Annex IX carries the information provided upon registration of testing in real world conditions and kept up to date thereafter, and lists five points: a Union wide unique single identification number of the testing, the name and contact details of the provider or prospective provider and of the deployers involved, a short description of the AI system and its intended purpose together with the information needed to identify it, a summary of the main characteristics of the testing plan, and information on the suspension or termination of the testing.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 49(4) and Annex IX","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"Article 60(4), point (c), provides that the provider or prospective provider has registered the testing in real world conditions in accordance with Article 71(4), with a Union wide unique single identification number and the information specified in Annex IX. For the systems referred to in points 1, 6 and 7 of Annex III in the areas of law enforcement, migration, asylum and border control management that registration takes place in the secure non-public section in accordance with Article 49(4), point (d), and for the systems referred to in point 2 of Annex III in accordance with Article 49(5). Article 60 sits in Chapter VI of the Regulation, on measures in support of innovation. That point (c) was not amended by Regulation (EU) 2026/1744.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 60(4), point (c), Article 49(4) and (5)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"The scope of Article 60 itself was amended. Article 1, point (24), of Regulation (EU) 2026/1744 replaces the first subparagraph of Article 60(1) and Article 60(2): testing in real world conditions outside AI regulatory sandboxes is now also open to providers and prospective providers of high-risk AI systems covered by the Union harmonisation legislation listed in Section A of Annex I, alongside the systems listed in Annex III. Article 1, point (25), inserts an Article 60a for high-risk AI systems covered by the harmonisation legislation listed in Section B of Annex I: Member States may adopt frameworks for real-world testing for those systems, must notify the Commission of any such framework before implementing it, and those frameworks must among other things ensure compliance with Article 60(2), (3), (4)(d)-(j) and (5)-(9). The registration duty in Article 60(4), point (c), which refers to Article 71(4), falls outside that enumeration.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Article 1, points (24) and (25), replacing Article 60(1), first subparagraph, and Article 60(2) and inserting Article 60a","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"Article 1, point (40), of Regulation (EU) 2026/1744 amends the THIRD paragraph of Article 113, which is where points (a) to (d) sit. Point (40)(b) replaces point (c) with: Chapter III, Sections 1, 2, and 3, with the exception of Article 6(5), applies from 2 December 2027 as regards AI systems classified as high-risk pursuant to Article 6(2) and Annex III, and from 2 August 2028 as regards AI systems classified as high-risk pursuant to Article 6(1) and Annex I. Two things belong with that and are often left out: the exception for Article 6(5) falls outside this deferral, and point (40)(c) adds a point (d) under which Articles 102 to 110 apply from 27 July 2026.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Article 1, point (40)(b) and (c), replacing Article 113, third paragraph, point (c) and adding point (d)","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"Recital 131 explains why the database exists and how far the public availability reaches. It names as the aim facilitating the work of the Commission and the Member States and increasing transparency towards the public, states that this part of the database should be publicly accessible and free of charge and that the information should be easily searchable, understandable and machine-readable, and that the database should be user-friendly, for example by offering search functionalities including through keywords, so that the general public can find the registration information. It adds that any substantial modification of high-risk AI systems should also be registered in the database, that access to the secure non-public section should be strictly limited to the Commission and, as regards their national section, to market surveillance authorities, and that the database should comply with the requirements of Directive (EU) 2019/882.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Recital 131","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"editorial_interpretation","text":"This is one of the few obligations in the Regulation whose output is a public page about your organisation. Article 53(1), point (d), is the other one: the provider of a general-purpose AI model makes public a summary of the training content used. The difference is that the database is your own entry rather than a document on your own site. The rest of your file opens only when a supervisory authority asks; this opens to anyone who can search. On machine readability a caveat applies: the Dutch text of paragraph 4 says the information must be machine-readable, the English says should, and Recital 131 likewise speaks in recommending terms. So count on your text being read, but do not build an assumption of automated readability as a hard requirement. That changes who reads your text. The basic and concise description of the operating logic in Section A is read by competitors, journalists and municipal councils, and the summary of your fundamental rights impact assessment in Section C is read by exactly the people that assessment was about, with one important exception: for points 1, 6 and 7 of Annex III the secure section carries Section C only up to and including point 3, so that very summary is not entered there. Two things follow. First, the entry requires editing rather than form filling: whoever writes the summary as a formality publishes a formality. Second, keeping it current is not a side issue, because Annex VIII requires the information to be kept up to date thereafter and Recital 131 also names substantial modifications, and an entry that still shows a recalled system as in service is visibly wrong.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Annex VIII, Sections A and C","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 49(4) and Annex IX","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Recital 131","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"recommended_action","text":"Treat the entry as a publication and not as a form. Designate per system the natural person who has the legal authority to register, because paragraph 5 provides that their name and contact details go into the database. Write the description of the intended purpose, of the operating logic and, for a public deployer, the summary of the fundamental rights impact assessment so that you can let them be read without explanation. Settle the sequence in your procurement contract: point 3 of Section C asks for the URL of the entry of the system in the database by its provider, so a municipality can only complete its Section C after its supplier has entered Section A. Record within what period the supplier delivers that URL and what happens if it does not. Also record when the entry was last checked against reality and tie that to your change and decommissioning process, so that status, Member States and declaration of conformity move with it. On procurement, check that the system is listed in the database before you put it into use: if it is not listed, a deployer may not use it under Article 26(8) and has to inform the provider or the distributor.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Annex VIII, Sections A and C","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 26(1)-(12)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}}],"legal_status":"upcoming","deadline_at":"2027-12-02T00:00:00.000Z","timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"public_page","href":"https://www.praxikon.com/en/verplichtingen/article-71-eu-database","label":"Open the human explanation"},{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 71 on EUR-Lex"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"source_verified","last_checked_at":"2026-08-14T00:00:00.000Z","next_review_due_at":"2027-02-10T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:obligation:article-99-101-penalties","legacy_id":"raip:obligation:article-99-101-penalties","type":"obligation","slug":"article-99-101-penalties","version":"1.0.0","effective_at":"2026-08-02T00:00:00.000Z","known_at":"2026-08-14T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"eebb183c9d9b58597388256d80ac73dc95eca9b9c98dd975ed907b55791e6905","label":"Article 99, 100 and 101: the penalty structure per obligation","summary":"The Regulation carries no single fine amount. For operators, three ceilings attach to different paragraphs of Article 99; in addition the Commission itself fines providers of general-purpose AI models under Article 101, the AI Office can fine in its own right since the 2026 amendment, and Union institutions and bodies face the separate amounts of Article 100. Which ceiling applies depends on which provision was infringed and on who enforces, and not on how serious the consequences are.","topics":["enforcement","prohibited-practices"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:distributor","praxikon:eu:ai-act:actor:gpai-model-provider","praxikon:eu:ai-act:actor:importer","praxikon:eu:ai-act:actor:provider"],"duty_holder_ids":[],"affected_actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:deployer","praxikon:eu:ai-act:actor:distributor","praxikon:eu:ai-act:actor:gpai-model-provider","praxikon:eu:ai-act:actor:importer","praxikon:eu:ai-act:actor:provider"],"oversight_actor_ids":["praxikon:eu:ai-act:actor:ai-office","praxikon:eu:ai-act:actor:market-surveillance-authority"],"evidence_owner_ids":[],"duty_holder_uncertainty_status":"out_of_scope","interpretation_status":"preliminary","interpretation_note":"Three things are unsettled here. First, whether an obligation not named in Article 99(3) to (5) carries a ceiling from the Regulation itself. We read Article 16, point (a), which obliges the provider to ensure that its high-risk systems comply with the requirements of Chapter III, Section 2, as meaning that non-compliance with Articles 9 to 15 by a provider is at the same time non-compliance with Article 16 and therefore sits inside the 3 percent ceiling, and Article 26 the same way for the deployer, including the duties that Article 26(5) draws in through Article 72 and Article 73. A defensible alternative reading is that the enumeration in paragraph 4 is meant strictly and covers only the duties written in Article 16 and Article 26 themselves, leaving the level for Articles 9 to 15 entirely to the national rules that paragraph 1 requires Member States to lay down. Second, what undertaking and total worldwide annual turnover in paragraphs 3 to 5 cover: the Regulation does not define this, and the difference between the turnover of the legal person fined and that of the group it belongs to is an order of magnitude in practice. We hold to the group reading because undertaking is construed that way in Union competition law, but that provenance is exactly the weak point: the Regulation nowhere refers to it, and the reading that the fined legal person is meant is equally defensible as long as there is no case law under this Regulation. Third, how far Article 75c(4) displaces the enumeration in paragraph 4: on its terms that provision governs enforcement by the AI Office over the operators of Article 75(1), and whether anything follows from it for the national route is unsettled. We read it narrowly, that is for the Office alone, and that is a reading and not settled law.","obligation_ids":[],"change_ids":[],"action_ids":["praxikon:eu:ai-act:action:article-99-101-map-penalty-tiers"],"evidence_ids":["praxikon:eu:ai-act:evidence:article-99-101-penalty-exposure-register"],"control_ids":["praxikon:eu:ai-act:control:article-99-101-mitigating-factor-record"],"template_ids":["praxikon:eu:ai-act:template:article-99-101-legal-text"],"conditions":[{"id":"article-99-101-penalties-scope","operator":"all","description":"Relevant as soon as you are an operator within the meaning of the Regulation, that is a provider, product manufacturer, deployer, authorised representative, importer or distributor, and one of the provisions named in Article 99(3), (4) or (5) is engaged. The Article 101 regime is additionally relevant where you are a provider of a general-purpose AI model, because there the Commission fines you itself. If you fall within the competence of the AI Office under Article 75(1), Article 75c is added on top."}],"exceptions":[{"id":"article-99-101-penalties-exception","operator":"not","description":"Paragraph 6 reverses the calculation for SMEs, including start-ups: for them the lower of the percentage and the amount applies, where for other undertakings it is the higher of the two, and it does so for every fine referred to in Article 99. The inserted paragraph 6a does the same for small mid-cap enterprises, but expressly only for paragraphs 4 and 5, so the Article 5 band is not reversed for them. Paragraph 8 leaves it to each Member State to determine to what extent administrative fines may be imposed on public authorities and bodies established in that Member State, so the ceiling for a public organisation does not follow from the Regulation. Paragraph 9 allows the fine to be imposed by the competent national courts or by other bodies rather than by the authority in some Member States."}],"statements":[{"kind":"official_fact","text":"Paragraph 1, as replaced by Regulation (EU) 2026/1744, requires Member States to lay down the rules on penalties and other enforcement measures, which may also include administrative fines, warnings and non-monetary measures, applicable to any infringement of this Regulation by operators, provides that those penalties shall be effective, proportionate and dissuasive, and requires Member States to take into account the interests of SMEs, including start-ups, and SMCs, and their economic viability when imposing penalties. Paragraph 2 requires Member States to notify those rules to the Commission without delay and at the latest by the date of entry into application, and to notify any subsequent amendment without delay. Paragraph 3 sets, for non-compliance with the prohibition of the AI practices referred to in Article 5, administrative fines of up to EUR 35 000 000 or, if the offender is an undertaking, up to 7 % of its total worldwide annual turnover for the preceding financial year, whichever is higher. Paragraph 4 sets, for non-compliance with provisions related to operators or notified bodies other than those laid down in Article 5, fines of up to EUR 15 000 000 or, if the offender is an undertaking, up to 3 % of that same turnover, whichever is higher, and enumerates: obligations of providers pursuant to Article 16, of authorised representatives pursuant to Article 22, of importers pursuant to Article 23, of distributors pursuant to Article 24, point (da) inserted by Regulation (EU) 2026/1744, obligations of providers and operators pursuant to Article 25(2) and (4), obligations of deployers pursuant to Article 26, requirements and obligations of notified bodies pursuant to Article 31, Article 33(1), (3) and (4) or Article 34, and transparency obligations for providers and deployers pursuant to Article 50. Paragraph 5 sets, for the supply of incorrect, incomplete or misleading information to notified bodies or national competent authorities in reply to a request, fines of up to EUR 7 500 000 or, if the offender is an undertaking, up to 1 % of that same turnover, whichever is higher. Paragraph 6 provides that in the case of SMEs, including start-ups, each fine referred to in this Article shall be up to the percentages or amount referred to in paragraphs 3, 4 and 5, whichever thereof is lower. The paragraph 6a inserted by Regulation (EU) 2026/1744 provides that in the case of SMCs, each fine referred to in paragraphs 4 and 5 shall be up to the percentages or amount referred therein, whichever is lower. Paragraph 7 enumerates what is taken into account when deciding whether to impose a fine and when deciding on the amount: the nature, gravity and duration of the infringement and of its consequences, whether administrative fines have already been applied by other market surveillance authorities to the same operator for the same infringement, whether other authorities have already fined that operator for infringements of other Union or national law resulting from the same activity or omission, the size, annual turnover and market share of the operator, any other aggravating or mitigating factor such as financial benefits gained or losses avoided, the degree of cooperation with the national competent authorities, the degree of responsibility of the operator taking into account the technical and organisational measures it implemented, the manner in which the infringement became known to the authorities and whether the operator notified it, the intentional or negligent character of the infringement, and any action taken by the operator to mitigate the harm suffered by the affected persons. Paragraph 8 provides that each Member State shall lay down rules on to what extent administrative fines may be imposed on public authorities and bodies established in that Member State. Paragraph 9 provides that, depending on the legal system of the Member State, the rules may be applied in such a manner that fines are imposed by competent national courts or by other bodies, with equivalent effect. Paragraph 10 subjects the exercise of these powers to appropriate procedural safeguards in accordance with Union and national law, including effective judicial remedies and due process. Paragraph 11 requires Member States to report annually to the Commission on the administrative fines they issued and on any related litigation or judicial proceedings. Chapter XII, which contains Article 99, has applied since 2 August 2025, with the exception of Article 101; the amendments to Article 99 have applied since 27 July 2026.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj","source_locator":"Article 99(1)-(11)"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj","source_locator":"Regulation (EU) 2026/1744, Article 1, point (38)"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj","source_locator":"Article 113, third paragraph, point (b)"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj","source_locator":"Regulation (EU) 2026/1744, Article 1, point (40)"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"Article 101(1) provides that the Commission may impose on providers of general-purpose AI models fines not exceeding 3 % of their annual total worldwide turnover in the preceding financial year or EUR 15 000 000, whichever is higher, where it finds that the provider intentionally or negligently infringed the relevant provisions of this Regulation, failed to comply with a request for a document or for information pursuant to Article 91 or supplied incorrect, incomplete or misleading information, failed to comply with a measure requested under Article 93, or failed to make available access to the model with a view to conducting an evaluation pursuant to Article 92. In fixing the amount of the fine or periodic penalty payment, regard shall be had to the nature, gravity and duration of the infringement, taking due account of the principles of proportionality and appropriateness, and the Commission shall also take into account commitments made in accordance with Article 93(3) or made in relevant codes of practice in accordance with Article 56. Paragraph 2 requires the Commission to communicate its preliminary findings to the provider and give it an opportunity to be heard before adopting the decision. Paragraph 3 provides that fines imposed shall be effective, proportionate and dissuasive. Paragraph 4 provides that information on fines imposed shall also be communicated to the Board as appropriate. Paragraph 5 gives the Court of Justice of the European Union unlimited jurisdiction to review decisions of the Commission fixing a fine and provides that it may cancel, reduce or increase the fine. Paragraph 6 requires the Commission to adopt implementing acts containing detailed arrangements and procedural safeguards for proceedings that may lead to a decision under paragraph 1. Article 101 is excluded from the earlier application of Chapter XII and has therefore applied since 2 August 2026. Alongside this regime, Article 100 carries its own scheme for Union institutions, bodies, offices and agencies: the European Data Protection Supervisor may impose administrative fines on them of up to EUR 1 500 000 for non-compliance with the prohibition in Article 5 and up to EUR 750 000 for non-compliance with other requirements or obligations under this Regulation. Regulation (EU) 2026/1744 did not amend Articles 100 and 101.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj","source_locator":"Article 101(1)-(6)"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj","source_locator":"Article 100(1)-(3)"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj","source_locator":"Article 113, third paragraph, point (b)"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"official_fact","text":"Article 75c(4), inserted by Regulation (EU) 2026/1744, provides that a decision of the AI Office may be accompanied by the imposition of penalties in accordance with Article 99(3) to (7), which provisions apply mutatis mutandis to the Office in the execution of its supervision and enforcement tasks referred to in Article 75(1). In particular, the following are subject to administrative fines as referred to in Article 99(4): infringement of any applicable provision of this Regulation, including those not listed in Article 99(4); failure to comply with decisions or measures adopted pursuant to Article 14(4) or Article 16(3) of Regulation (EU) 2019/1020 and the powers specified in Article 75a; and failure to comply with a commitment made binding pursuant to Article 75b. The supply of incorrect, incomplete or misleading information to the Office is subject to the fines of Article 99(5). Paragraph 5 additionally allows the Office to impose periodic penalty payments to compel, among other things, submission to an investigation, compliance with an information request, submission to an inspection or compliance with a binding commitment; those payments shall not exceed 5 % of the average daily income or worldwide annual turnover in the preceding financial year per day. Paragraph 6 gives the Court of Justice unlimited jurisdiction over decisions of the Office fixing a fine or periodic penalty payment, and paragraph 8 subjects the powers of the Office to a limitation period of five years, with the same period for the power to enforce decisions taken. Note: the two authentic language editions of Regulation (EU) 2026/1744 diverge here. The English edition states five years in both subparagraphs of Article 75c(8); the Dutch edition states three years in both subparagraphs of Article 75 quater(8). This statement renders in each language what the edition in that language says and makes no silent choice. The implementing act under Article 75d(3) is to specify both subparagraphs, including the circumstances in which the limitation periods are interrupted; until it exists, the divergence remains an open question of interpretation.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj","source_locator":"Regulation (EU) 2026/1744, Article 1, point (32)"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"editorial_interpretation","text":"The ceiling follows the provision, not the harm. That is the point routinely missed in boardrooms: a single amount gets budgeted for \"the AI Act fine\", while operators face three bands in Article 99 and there are separate regimes on top for Union institutions and for providers of general-purpose AI models. The highest band, EUR 35 million or 7 percent, belongs to Article 5 alone. Until recently that was a list of practices you either engage in or do not, but since the amendment of Article 5 that is no longer true: for the new prohibitions on sexual imagery, placing on the market is also prohibited where such generation is a reasonably foreseeable and reproducible outcome and the system lacks reasonable and adequate technical safety measures and safeguards. That is a duty to take measures inside the highest band, and it applies from 2 December 2026. The middle band, EUR 15 million or 3 percent, belongs to the enumeration in paragraph 4: the role duties of the provider, the authorised representative, the importer, the distributor and the deployer, since 27 July 2026 also Article 25(2) and (4), plus Article 50. What is not named there is at least as interesting: Article 4 and Article 27 do not appear, and the requirements of Chapter III reach the ceiling at most through Article 16 and Article 26. Note that Article 72 and Article 73 do come within reach for the deployer, because Article 26(5) obliges it to inform in accordance with Article 72 and declares Article 73 applicable mutatis mutandis, and Article 26 is named in paragraph 4. Two further things. Paragraph 5 turns answering an information request badly into its own fine category at 1 percent, independently of the underlying infringement. And paragraph 7 is not a discount scheme: it works both ways, because its opening words concern the decision whether or not to impose a fine and point (e) expressly names aggravating factors such as financial benefits gained. What you can steer are the factors you can evidence: your technical and organisational measures, your notification behaviour, your cooperation, and what you did after an incident to mitigate the harm suffered by affected persons. Two dates that matter in practice: the prohibition in Article 5 has applied since 2 February 2025 but Chapter XII only since 2 August 2025, so for conduct in between there is no administrative fine under Article 99(3). That gap does not return for the new Article 5 prohibitions of 2 December 2026: Chapter XII will by then have applied for well over a year, so the penalty regime exists on the day those prohibitions start to apply. And whoever falls within the competence of the AI Office must drop the idea that the enumeration in paragraph 4 is closed: Article 75c(4) places infringement of any applicable provision in the EUR 15 million or 3 percent band there, expressly including provisions not listed in paragraph 4.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj","source_locator":"Article 99(1)-(11)"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj","source_locator":"Regulation (EU) 2026/1744, Article 1, point (7)"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj","source_locator":"Regulation (EU) 2026/1744, Article 1, point (32)"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj","source_locator":"Article 113, third paragraph, point (b)"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"recommended_action","text":"Add a column to your obligations register carrying the ceiling that belongs to each entry, with three values: Article 99(3), Article 99(4), or national law under Article 99(1). Determine per general-purpose AI model that you provide yourself whether the Commission's Article 101 regime is added on top, and determine whether you fall under Article 75(1), because the Article 75c regime with periodic penalty payments then applies as well. Also record, per obligation, which of the factors in Article 99(7) you could actually show, in particular the technical and organisational measures implemented, your notification behaviour, your cooperation with the authority and the steps you take to mitigate harm to affected persons, because that is the part of the amount you can influence yourself. This is our recommendation and not a duty under the Regulation: Article 99 addresses the Member States and imposes no deadline whatsoever on an operator.","citations":[{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj","source_locator":"Article 99(1)-(11)"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj","source_locator":"Article 101(1)-(6)"},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj","source_locator":"Regulation (EU) 2026/1744, Article 1, point (32)"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}}],"legal_status":"applicable","deadline_at":null,"timing_basis":null,"high_risk_regime_from":null,"links":[{"relation":"public_page","href":"https://www.praxikon.com/en/verplichtingen/article-99-101-penalties","label":"Open the human explanation"},{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","label":"Article 99, 100 and 101 on EUR-Lex"},{"relation":"official_source","href":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","label":"Regulation (EU) 2026/1744, the amendment of Article 99"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"},"source_review":{"level":"source_verified","last_checked_at":"2026-08-14T00:00:00.000Z","next_review_due_at":"2027-02-10T00:00:00.000Z","date_basis":"first_publication"}},{"id":"praxikon:eu:ai-act:standard:standard-pren-18285-conformity-assessment-framework","legacy_id":"raip:standard:standard-pren-18285-conformity-assessment-framework","type":"standard","slug":"standard-pren-18285-conformity-assessment-framework","version":"1.0.0","effective_at":"2026-08-08T00:00:00.000Z","known_at":"2026-08-08T00:00:00.000Z","valid_until":null,"payload_hash_sha256":"6912ad1f00cd9830b1995fd9ea6e88df0aeb116adb20a4655378cb061d173ff0","label":"prEN 18285: conformity assessment framework for AI systems","summary":"The draft European standard operationalising the conformity assessment procedure of Article 43 and Annex VII.","topics":["standards"],"actor_ids":["praxikon:eu:ai-act:actor:authorised-representative","praxikon:eu:ai-act:actor:provider"],"duty_holder_ids":[],"affected_actor_ids":[],"oversight_actor_ids":[],"evidence_owner_ids":[],"duty_holder_uncertainty_status":null,"interpretation_status":null,"interpretation_note":null,"obligation_ids":["praxikon:eu:ai-act:obligation:conformity-ce-registration"],"change_ids":[],"action_ids":[],"evidence_ids":[],"control_ids":[],"template_ids":[],"conditions":[{"id":"standard-pren-18285-conformity-assessment-framework-scope","operator":"all","description":"The Article 43 conformity assessment rests on the provider. The authorised representative established in the Union keeps the EU declaration of conformity and the technical documentation available to the supervisory authority and cooperates with it under Article 22."}],"exceptions":[],"statements":[{"kind":"official_fact","text":"prEN 18285 (Conformity assessment framework) is the JTC 21 deliverable under M/613 covering the conformity assessment of high-risk AI systems under Article 43 and Annex VII of the AI Act. As at June 2026 the deliverable was at the drafting stage. It has not yet been published as an EN and is not cited in the Official Journal. Standardisation request M/613 was amended by Implementing Decision C(2025)3871 of 23 June 2025 and expires on 28 February 2027.","citations":[{"source_id":"praxikon:eu:ai-act:source:cen-cenelec-jtc21","source_locator":"prEN 18285 (draft standard), CEN/CLC/JTC 21 under M/613","source_url":"https://www.cencenelec.eu/areas-of-work/cen-cenelec-topics/artificial-intelligence/","eli":null},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 43 and Annex VII; Article 22; Article 40","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"source_checked"}},{"kind":"editorial_interpretation","text":"This is the deliverable that determines how heavily the rest weighs. For most Annex III systems the provider may self-assess (internal control), but that does not mean nothing is required: it means you must be able to show the complete dossier yourself. The trap is thinking self-assessment is light. The notified body is absent, the burden of proof is not. While prEN 18285 remains in draft, there is no recognised blueprint for that self-assessment and you must justify the structure yourself.","citations":[{"source_id":"praxikon:eu:ai-act:source:cen-cenelec-jtc21","source_locator":"prEN 18285 (draft standard), CEN/CLC/JTC 21 under M/613","source_url":"https://www.cencenelec.eu/areas-of-work/cen-cenelec-topics/artificial-intelligence/","eli":null},{"source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 43 and Annex VII; Article 22; Article 40","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}],"review":{"reviewed_at":"2026-08-08T00:00:00.000Z","reviewer":"Praxikon release validation","review_method":"source_link_and_rule_validation","legal_status":"editorial"}},{"kind":"recommended_action","text":"Determine per system which assessment route applies (internal control or notified body) and build your dossier as one an external party would have to be able to read, even where you self-assess. 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