Professional EU AI Act Scope Review
Get a fact-specific view of your EU AI Act exposure before building the compliance program.
The review is designed for U.S. companies that need to clarify applicability, actor role, classification and priority obligations around one or more real AI systems.
What to send
Start with the facts that change the legal analysis.
You do not need a polished memo. A short description of the system, your role and the EU connection is enough to determine whether a professional scope review is appropriate.
Useful information to include
- Company and principal market.
- AI product or use case.
- Whether you develop, provide, deploy or resell the system.
- EU customers, users, employees or affected persons.
- Whether generative AI or GPAI models are involved.
- Any HR, education, biometric, credit, insurance, infrastructure or other sensitive use.
- Your target launch/compliance date.
What the review is designed to answer
A defined first decision, not an open-ended compliance project.
Applicability
Does Article 2 bring the company or relevant activity within scope?
Actor role
Is the company acting as provider, deployer or another regulated participant?
Classification
Are Article 5, Article 50, GPAI or high-risk pathways relevant?
Next actions
What needs to be documented, fixed or escalated next — and what can wait?
The exact scope, deliverables, timing and commercial terms are agreed before an engagement begins.
Before the call
You can run the scoping questions first.
The assessment is designed to structure the facts, not to issue an automatic legal conclusion.