EUDAMED becomes mandatory: What medical device companies need to prepare in less than 6 months

The clock is ticking: In exactly six months, EUDAMED will become mandatory – and this has now been officially confirmed. From May 28, 2026, all new medical devices must be registered in EUDAMED before they can be placed on the market in Europe. For products already on the market, the deadline is November 28, 2026. But that’s just the beginning: The European Commission also plans to make vigilance modul mandatory from Q2 2027.

In this webinar, you will learn: 

• What these deadlines mean for your company
• Which steps you need to prioritize now
• How to set up your EUDAMED implementation process efficiently.

Benefit from best practices, compact expert knowledge, and a clear implementation roadmap—so you can confidently master the upcoming regulatory milestones.