The MDIA is hosting an information session for healthcare and MedTech stakeholders on the impact of the EU AI Act on AI-enabled medical technologies.

This session will:

✅ Clarify how the EU AI Act interacts with the MDR and IVDR frameworks

✅ Explain how AI-powered medical devices and healthcare solutions may be considered high-risk

✅ Outline key obligations for manufacturers, providers, deployers, and other economic operators

✅ Highlight recent developments under the Digital Omnibus on AI and include a live Q&A

Attendees will gain practical insights to help integrate AI Act requirements into existing compliance processes and prepare for upcoming regulatory obligations.

📅 17 July 2026 | 14:00 – 17:00 | Hybrid

Stay informed. Stay compliant.