With the MDR, EUDAMED will act as central repository of information to lay the foundation for collaboration, transparency and interaction of all parties, namely the new European databank for medical devices and in vitro diagnostic devices.
EUDAMED will have several modules and contain extensive data. The data will allow access to all stakeholders including the European Commission, NCAs, Notified Bodies, MAID, Sponsors and the public.
Registration will be open to Economic Operators starting in December 2020
Do you know how to register for EUDAMED?
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Read Meditrial’s whitepaper to learn more on the MDR and Eudamed.
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Table of Contents
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This article provides general information and does not constitute regulatory, legal, clinical, or compliance advice. Requirements and appropriate processes may vary by study, product, jurisdiction, and organization. Medigen Suite functionality should be used in accordance with applicable regulations, study documentation, and internal procedures.
