Authorised Representative services for non-EU providers of high-risk AI systems and GPAI models.
Find out which companies and AI systems fall under the mandatory Authorised Representative requirement.
Discover the key reasons non-EU companies must appoint an Authorised Representative.
Understand the core legal responsibilities every Authorised Representative must fulfill.
A detailed breakdown of the day-to-day tasks an AR performs on behalf of providers.
Interactive Article 3(1) assessment to determine whether your system is an AI system under the EU AI Act.
Guided risk classification: prohibited practices, high-risk routes, Article 6(3) derogation, and transparency obligations.
Comprehensive gap analysis and prioritised roadmap to achieve full compliance.
ISO/IEC 42005-aligned impact assessment tools supporting Article 9 risk management and conformity.
Fully auditable Quality Management System aligned with Article 17 and EN 18286.