100 Days to EUDAMED: The countdown to the deadline starts now

EUDAMED is approaching fast. From May 28, 2026, EUDAMED becomes the legally required system for key Medical Devices Regulation (MDR) and In Vitro Diagnostic Medical Devices Regulation (IVDR) processes.  The transition period is short. Late preparation increases the risk of losing market access, income, customers, and partners.  

This webinar focuses on what EUDAMED requires now, which obligations apply to your role in the supply chain, and how to prepare efficiently. 

In this webinar, you will learn: 

• What the EUDAMED database is and what changes in 2026 
• The key deadlines and who has to comply
• A practical preparation approach for the final 100 days 
• Live Q&A 

If you are responsible for regulatory compliance, UDI and device data, quality management, or EU market access, this session will help you move from awareness to action.