QARA Bitesize – EUDAMED (Part 2)
The European Database on Medical Devices (EUDAMED) is a centralised EU database for the registration and monitoring of medical devices. It is a core element of the implementation of the Medical Device Regulation and the In Vitro Diagnostic Regulation, providing a collaborative and interoperable platform for registration and reporting.
With the first four EUDAMED modules becoming mandatory from 28 May 2026, this webinar will examine the current state of play, industry preparedness, and expectations regarding EUDAMED. It will outline what organisations must do to remain compliant and avoid delays.
In this session, we will hear from speakers from the European Commission, TÜV SÜD, and Johnson & Johnson/MedTech Europe providing a full, cross stakeholder perspective on the process.
Full list of speakers:
• Marina Madokoro - Regulatory Affairs Manager, UDI EMEA, Johnson & Johnson - Chair of EUDAMED Working Group, MedTech Europe
• Pierre-Francois Ryelandt - Policy Officer, European Commission
• Marta Carnielli - Head of Certification IVD, TÜV SÜD
• Norbert Baranowski - Process Owner Certification, TÜV SÜD
• Toma Pervan - Executive, Irish Medtech
Members enjoy access to our online HR Management Guide offering sample documents, guidance, research, FAQs and articles. Members also receive premium HR services and supports, networking events and preferential rates for conferences and Ibec Management Training accredited programmes and short courses.
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