Your mandated EU point of contact under Article 22 of the AI Act
Explainers and starting points for non-EU providers preparing for high-risk AI market access.
Detailed guides on specific AI Act obligations.
Triage for providers, SaaS companies and AI service teams entering the EU market.
Start here if you are unsure whether Article 22 applies.
Annex III categories and screening questions.
Key dates after Regulation (EU) 2026/1744.
What the authorised representative role does and does not do.
If the AI system is embedded in a physical product, the underlying product regulation is a separate role from Article 22:
MDR/IVDR Article 11, on getEAR.eu.
Conformity assessment strategy for medical devices, on getMDR.eu.
For non-medical regulated products, on getCE.eu.
For non-CE consumer products, on getGPSR.eu.
For cosmetic products, on getCosmeticRP.eu.
For chemical substances, on getREACHOR.eu.
Tell us where the provider is established, what the AI system does, and whether Annex III may apply. Before you sign an appointment mandate, we tell you what the next step is.