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#EU-ACT-ART-22|HIGH RISK
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Article 22: Authorised Representatives of Providers of High-Risk AI Systems

Official Statutory Text

Article 22 Authorised representatives of providers of high-r isk AI systems 1. Prior to making their high-r isk AI systems available on the Union mark et, providers established in third countries shall, by written mandate, appoint an authorised representative which is established in the Uni on. 2. The provider shall enable its authorised representative to perform the tasks specified in the mandatereceived from the provider . 3. Theauthorised representative shall perform the tasks specified in the mandatereceived from the provider . It shall providea copy of the mandate to the market surveillanceauthorities upon request, in one of the official languages of the institutions of the Union, as indicated by the competent authority . For the purposes of this Regulation, the mandate shall empower theauthorised representative to carry out the following tasks : (a) verify that the EU declaration of conformity refer red to in Article 47 and thetechnical documentation referred to in Article 11 have been drawn up and that an appropriate conformity assessment procedure has been carried out by the provider ; (b) keep at the disposal of the competent authorities and national authorities or bodies referred to in Article 74(10), for a period of 10 years after the high-r isk AI system has been placed on the marketor put into service, the contact details of the provider that appointed theauthorised representative, a copy of the EU declaration of conformity refer red to in Article 47, thetechnical documentation and, if applicable, the certificate issued by the notified body ; (c) providea competent authority , upon a reasoned request, withall the information and documentation, including that referred to in point (b) of this subparagraph, necessary to demonstrate the conformity of a high-r isk AI system with the requirements setout in Section 2, including access to the logs, as referred to in Article 12(1), automatically generated by the high-r isk AI system, to the extent such logs are under the control of the provider ; (d) cooperate with competent authorities, upon a reasoned request, in any action the latter take in relation to the high-r isk AI system, in particular to reduceand mitigatetherisks posed by the high-r isk AI system; (e) whereapplicable, comply with the registration obligations refer red to in Article 49(1), or , if the registration is carried out by the provider itself, ensure that the information refer red to in point 3 of Section A of Annex VIII is cor rect. The mandate shall empower theauthorised representative to beaddressed, in addition to or instead of the provider , by the competent authorities, on all issues related to ensuring compliance with this Regulation. 4. Theauthorised representative shall terminate the mandate if it considers or has reason to consider the provider to beacting contrary to its obligations pursuant to this Regulation. In sucha case, it shall immediately inform the relevant market surveillanceauthority , as well as, whereapplicable, the relevant notified body , about thetermination of the mandateand the reasons therefor .

Legal Authority

European Parliament & Council (Regulation 2024/1689)

View Official EUR-Lex Publication
Mandatory Statutory Checklist & Fix
  • For providers established in third countries: Prior to making high-risk AI systems available on the Union market, appoint an authorised representative established in the Union via a written mandate.
  • Enable your authorised representative to perform the tasks specified in their mandate.
  • For authorised representatives: Ensure your mandate empowers you to verify that the EU declaration of conformity (Art. 47) and technical documentation (Art. 11) have been drawn up and the appropriate conformity assessment procedure has been carried out.
  • Keep at the disposal of competent authorities (for 10 years after market placement/service) the provider's contact details, a copy of the EU declaration of conformity, technical documentation, and, if applicable, the certificate issued by the notified body.
  • Provide competent authorities, upon a reasoned request, with all necessary information and documentation, including access to logs (Art. 12(1)) if under provider control, to demonstrate conformity.
  • Cooperate with competent authorities in any action to reduce and mitigate risks posed by the high-risk AI system.
  • Comply with registration obligations (Art. 49(1)) or ensure the correctness of information if the provider carries out registration.
  • Ensure your mandate allows competent authorities to address you on all compliance issues, in addition to or instead of the provider.
  • Terminate the mandate immediately if you consider the provider to be acting contrary to their obligations, and inform the relevant market surveillance authority (and notified body, if applicable) of the termination and reasons.
Statutory Classification
HIGH RISK

Applies directly across all 27 EU Member States with phased entry into force from 2025 to 2026.