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


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


Yves Despres

Senior Director, Regulatory affairs, Medical, EMEA, MECOMED


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.