Watch now: EUDAMED explained and what’s coming
Watch this informative and practical webinar to learn more about the European Database on Medical Devices (EUDAMED), a cornerstone of the EU Medical Devices Regulation (MDR) and In Vitro Diagnostic Medical Devices Regulation (IVDR).
Webinar date
May 28, 2026
Speaker
Tom Ingless, senior quality and regulatory affairs consultant, Emergo by UL
EUDAMED compliance
Designed to increase transparency, traceability and regulatory oversight, EUDAMED brings together actor registration, unique device identifier (UDI) data, certificates, clinical investigations, vigilance and market surveillance into a single, interconnected system.
While not all EUDAMED modules are yet mandatory, regulators and notified bodies increasingly expect companies to be EUDAMED-ready. With several modules already live and transition periods moving quickly, manufacturers have limited time to prepare.
What you’ll learn in this webinar
- What EUDAMED is, how the database is structured and how each module works
- EUDAMED obligations that apply now
- Implementation timelines
- EUDAMED readiness gaps seen across the industry
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