EU AI Act support / AI compliance (EU)

Practical guidance for AI providers and deployers under the EU AI Act — including documentation readiness, risk classification support, and EU representation considerations for non‑EU companies.

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What the EU AI Act changes

The EU AI Act (Regulation (EU) 2024/1689) introduces obligations for providers and deployers of AI systems and certain AI models. Applicability depends on your role (provider/deployer/importer/distributor) and on the AI system category (e.g., high-risk).

If AI is used in or with medical devices, MDR/IVDR obligations may also apply in parallel.

Typical topics we cover

Role & scope

Clarify whether you act as provider, deployer, distributor, etc.
Map the AI system to the main AI Act obligations (high-level)
Identify cross‑regulation overlaps (e.g., MDR/IVDR)

Documentation readiness

Outline required documentation blocks (as applicable)
Support with evidence structure and internal ownership
Set up a workflow for updates and change control

EU representation considerations

For non‑EU providers, EU rules may require an authorised representative in the EU for placing AI systems on the EU market
Define contact point and authority request handling workflow
Align public-facing information and compliance communication

Related services

Need a quick AI Act scope check?

Send a short description of your AI product, target markets, and your role (provider/deployer) — we’ll confirm the likely scope and next steps.

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