In this in-depth webinar, experts from Nemko Digital unpack the EU AI Act’s new risk-based framework and guide organisations through the critical steps of conformity assessment.

You’ll learn how AI systems are classified—from prohibited and high-risk to limited- and low-risk—and why high-risk applications (embedded in regulated products or used in sensitive areas such as education, healthcare, and law enforcement) must obtain CE marking before entering the EU market.

The session clarifies provider and deployer obligations, explains the difference between self-assessment (internal control using harmonized standards) and third-party notified-body reviews, and walks through real-world examples including medical devices, biometric systems, and general-purpose AI integrations.

The presenters also share a practical “Step 0” checklist: identify your AI use cases, assess risk levels, determine your role, choose the appropriate assessment route, and begin preparing quality-management systems and technical documentation today.

You’ll get an exclusive look at Nemko Digital’s AI Trustmark process—a structured pathway from awareness and in-house consultation to risk categorization and a formal evaluation report—that helps companies not only comply with the EU AI Act, but also build market credibility and stakeholder trust.

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