AI Act role · Art. 3(8)
EU AI Act — Authorised representative
You are appointed in writing by a non-EU provider to perform specified tasks on their behalf to comply with the AI Act.
Key obligations apply from
2 August 2026
Risk tier
high risk
Full AI Act applies by Aug 2027 for remaining Annex I scope
Scope notes: Authorised representatives must hold a mandate, verify conformity documentation, and cooperate with authorities — and may be liable alongside the provider for defective systems.
First steps before 2 August 2026
- 1Execute written mandate covering Art. 22 tasks
- 2Maintain access to technical documentation and conformity records
- 3Register high-risk AI in the EU database where mandated
Who supervises you?
Market surveillance authorities in each Member State enforce the AI Act. The European AI Office supports coordination, GPAI oversight, and cross-border cases.
AI Act implementation & AI OfficePriority mandates for you
2 instrumentsEU database registration — high-risk AI
Implementing act on registration in the EU database for high-risk AI systems before placement on the market.
Why it matters: Public register of high-risk AI — providers must register with prescribed information before going live.
View on mapHigh-risk AI systems — requirements and conformity
Guidelines on the practical implementation of Chapter III requirements — risk management, data governance, transparency, human oversight, accuracy, and robustness (Art. 96(1)(a)).
Why it matters: Primary interpretive guide for Chapter III conformity once published — distinct from the Art. 6 classification consultation now open.
View on mapThis page is an independent orientation guide — not legal advice. National implementation and sector-specific rules may apply. Always verify scope against the official AI Act text and your supervisor.