Are you ready for the EU AI Act? Take the Articles 22 & 49 Health Check.

1.Does your organisation deploy or use AI systems within the EU market (including AI systems developed outside the EU)?

2.Have you classified all your AI systems by risk category (unacceptable, high-risk, limited, minimal) as required under the EU AI Act?

3.For any high-risk AI systems, have you established a comprehensive risk management system in accordance with Article 9?

4.Do you have an appointed Authorised Representative within the EU for high-risk AI systems placed on the market from outside the EU, as required by Article 22?

5.Has your Authorised Representative been given a written mandate specifying the tasks they must perform on your behalf under Article 22(3)?

6.Is your Authorised Representative able to provide the national competent authority with a copy of the EU declaration of conformity and technical documentation upon request?

7.Have you registered your high-risk AI systems, and your Authorised Representative's details, in the EU database as required by Article 49?

8.Does your EU database registration include all mandatory information listed in Annex VIII (system description, manufacturer details, conformity status, member states of use)?

9.Do you have processes in place to keep your Article 49 database registration up-to-date whenever there are material changes to your AI systems?

10.Are you aware that high-risk AI obligations — including the Article 22 Authorised Representative and Article 49 registration requirements — apply from 2 December 2027, and do you have a compliance roadmap to meet it?