The European Commission announced the activation of the modules on UDI/device registration (second module) and on Certificates and Notified Bodies (third module) by September 2021. The first module on Actor registration is available since December 2020.
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.
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.
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Highly descriptive article, I enjoyed that bit.
I would suggest checking Mastertrial. Provided some good training modules for all sorts of regulatory topics
Hi Phil,
To learn further about our training please check out Mastertrial.com
Thanks,
Meditrial Helpline
Interested in the trainings on UDI and EUDAMED. Please share fee information