Medical Devices
4th December
How to implement the transition to the new European medical device regulation?
Details :
- Organization by videoconference (Zoom)
Participants: members of the Algerian Medicines and Pharmaceuticals Agency, Ministry of Pharmaceutical Products, Center of Pharmacovigilance
Recording of the session
Outcomes
This session helped the algerian agency gain a better understanding of what the new MDR, Medical Device Regulation, will imply and the upcoming changes to prepare at best.
A more thorough Q&A session has followed the session
Speakers
- Yves Despres - Senior Director, Regulatory affairs, Medical, EMEA, MECOMED
Yves Despres
Senior Director, Regulatory affairs, Medical, EMEA, MECOMED
Acknowledgements
This training was possible thanks to the support and participation of our partner MECOMED , medical devices, imaging and diagnostics trade association across the Middle East & Africa (MEA) with the content of the seminar as well as our sponsor (without conditions) BD.
