The European Commission’s high-level conference “Medical Devices: Innovation and Patient Safety”, held on 16 March 2026 in Brussels, is now available to watch on demand.
The event addressed the Commission’s proposed revision of the MDR (Regulation (EU) 2017/745) and IVDR (Regulation (EU) 2017/746), with sessions covering conformity assessment predictability, the role of Expert Panels, and the regulatory framework for breakthrough technologies — all areas of active legislative development.
The recording offers a useful overview of the Commission’s current policy direction for those who could not attend in person.
Access the recording via the European Commission’s health website.
Source: European Commission
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