‘Eudamed is the database established under Regulation (EU) 2017/745 on medical devices and Regulation (EU ) 2017/746 on in vitro diagnostic medical devices.‘
European Commission
Did you have to read it twice? You wouldn't be alone if you did! And in that case, you're in good hands with us!
Because in 2025, BEO BERLIN will offer a new series of workshops on the topic of EUDAMED! Our offer is aimed at manufacturers of medical devices and offers you the opportunity to obtain comprehensive information about the latest developments and requirements of the European Database for Medical Devices (EUDAMED).
What can you expect?
Our in-house experts, as well as highly qualified partners of BEO BERLIN, will guide you through the following topics in this series of workshops:
- In-depth insights into the functions and requirements of EUDAMED
- Practical instructions for registering and using the database
- Exchange with experts and other industry players
- Deadlines, case studies and best practices are presented.
Dates and locations
We are still in the planning phase and will be able to announce dates and locations soon.
Are you interested in this topic? Would you attend our workshop? Would you like to see more topics covered in our workshops? Then get in touch!
To stay up-to-date, subscribe to our newsletter, so as not to miss the start of the workshops and our other news. Take this opportunity to expand your knowledge and prepare yourself optimally for the challenges of EUDAMED. We look forward to receiving your feedback and to welcoming you to our workshops!
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