How to implement the transition to the new European medical device regulation?
- Organization by videoconference (Zoom)
Participants: members of the Algerian Medicines and Pharmaceuticals Agency, Ministry of Pharmaceutical Products, Center of Pharmacovigilance
Recording of the session
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
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.