EUDAMED onboarding webinars

The central medical device database, EUDAMED – a key EU medical device regulatory infrastructure – will become mandatory from 28 May 2026. Preparing for EUDAMED readiness requires a cross-functional transformation, involving teams across regulatory affairs, quality, R&D,  labelling, product data management and commercial functions.

• To support senior business leaders in understanding the strategic implications, MedTech Europe hosted a high-level “Executives’ Overview of EUDAMED” webinar. The 30-min session highlights the key aspects of EUDAMED that influence executive decision-making and organisational readiness.

• A MedTech Europe technical deep-dive webinar on EUDAMED UDI/Device registration was designed to support companies preparing for EUDAMED data submission, combining regulatory context with practical operational guidance.

Part 1

Part 2

The webinar recordings and presentation of the executives’ EUDAMED overview and the technical deep-dive on device registration webinars are available for download below.