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?
Contact Meditrial to learn everything you need to know on how to prepare! With us, you will be the first to comply.
Read Meditrial’s whitepaper to learn more on the MDR and Eudamed.
Sign up to Meditrial Academy course offerings to find free training and opportunities for professional certification.
Contact Meditrial for immediate assistance in Europe or the US.
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