MedTech Europe EUDAMED training available

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 has hosted a high-level “Executives’ Overview of EUDAMED” webinar. The 30-min session highlighted the key aspects of EUDAMED that influence executive decision-making and organisational readiness.

A two-part technical deep-dive webinar on EUDAMED UDI/Device registration (Part 1 / Part 2), designed to support companies preparing for EUDAMED data submission, combining regulatory context with practical operational guidance, was also hosted by MedTech Europe.

Two pdf downloads have also been made available by MedTech Europe:

• Executives’ overview of EUDAMED
• MedTech Europe EUDAMED Training