FREE WEBINAR | EUDAMED MODULE 2

After a long wait, on October 4th, 2021, the European Commission made the UDI/Device Registration module 2 of Eudamed available.

November 2, 2021

When? 📆 17/11/2021 🕛 3:00 p.m. (CET)

Are you ready for the new challenges EUDAMED Module 2 poses?

After a long wait, on October 4th, 2021, the European Commission made the UDI/Device Registration module 2 of Eudamed available.

This means that Medical Device manufacturers are now able to upload all the information related to their MDR devices on a voluntary basis until 6 months after Eudamed being fully functional, when it will become mandatory.

Join Asphalion expert Fran Rodríguez in this webinar where the newest updates on EUDAMED will be addressed:

Brief overview of Eudamed
Go live of Module 2 of Eudamed
UDI codes and implementation timelines
Management of legacy devices
Data submission related to this module
Q&A

For further information you can contact us at: [email protected]

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FREE WEBINAR | EUDAMED MODULE 2

After a long wait, on October 4th, 2021, the European Commission made the UDI/Device Registration module 2 of Eudamed available.

Search

Filter by category

Related news and events

New Guidance on the Interplay Between the MDR/IVDR and the Artificial Intelligence Act (AIA)

VIDEO | Key dates in the Regulatory Landscape for the MedTech Industry

NEWS | New MDGC Guidance on MDSW

About

Team

Partners

CSR

AI Ethic Code

Careers

FREE WEBINAR | EUDAMED MODULE 2

After a long wait, on October 4th, 2021, the European Commission made the UDI/Device Registration module 2 of Eudamed available.

Search

Filter by category

Related news and events

New Guidance on the Interplay Between the MDR/IVDR and the Artificial Intelligence Act (AIA)

VIDEO | Key dates in the Regulatory Landscape for the MedTech Industry

NEWS | New MDGC Guidance on MDSW

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