When Do You Must Comply?
The deadline for high-risk AI system providers is 2 August 2026. For GPAI model providers, obligations have already applied since 2 August 2025.
AUTHORISED REPRESENTATIVE IN EU FOR NON-EU AI PROVIDERS
Non-EU providers of high-risk AI systems and general-purpose AI models must appoint an EU-established Authorised Representative before placing their products on the European market. eyreACT provides that representation, backed by regulatory lawyers who helped draft the law.
The Authorised Representative obligation under Articles 22 and 54 of EU AI Act is a market access condition. Providers without a properly mandated EU representative face fines of up to EUR 15,000,000 or 3% of global annual turnover, whichever is higher, and cannot lawfully operate in the EU market.
The deadline for high-risk AI system providers is 2 August 2026. For GPAI model providers, obligations have already applied since 2 August 2025.
Non-compliance with the AI Act's representation requirements is not just a technical oversight regulators overlook. These are the four primary risks non-EU providers face.
Appointing a representative after the deadline does not erase the period of non-compliance. Regulators assess liability from the date the obligation first applied.
Providers of high-risk AI systems under Annex III must have a mandated EU representative in place before 2 August 2026, with no grace period after that date.
If your general-purpose AI model has been on the EU market since August 2025, the obligation to appoint an Authorised Representative applies now.
Each failure to comply is assessed separately. A provider operating multiple AI systems without representation faces cumulative exposure across each product.
The European AI Office and national market surveillance authorities are actively issuing guidance and preparing for enforcement, not waiting for the transition period to expire.
Post-Brexit, a UK-based entity cannot serve as an EU Authorised Representative. Providers who have relied on UK legal counsel or a UK subsidiary to fulfil this role are not compliant.
Any third-country (USA, Canada, UK, China, MENA) provider whose AI system forms a safety component in an Annex I regulated product as well as:
Most Authorised Representative services offer a named address and a filing cabinet. eyreACT operates differently because the role demands it. We offer regulatory-grade representation, built on the compliance infrastructure the role actually requires.
eyreACT is built by European regulatory lawyers. We understand what market surveillance authorities expect when they make a request, and we respond accordingly.
Our compliance engine reviews your technical documentation against the AI Act's requirements before we accept the mandate. We do not sign off on documentation we have not assessed.
All technical documentation within scope are held in eyreACT's secure compliance infrastructure for the full 10-year retention period, accessible to authorities on request.
The AI Act is a living framework. eyreACT tracks regulatory updates, Commission guidance, AI Office decisions, and harmonised standards as they are adopted, and notifies you when your documentation or system requires updating.
Appointment must precede market placement. Providers who have already placed systems on the EU market without a properly mandated representative should seek advice without delay. Book a consultation to let us assess your AI systems, confirm the applicable deadline, and issue a draft mandate within five working days.