Medical Devices Regulation

16-17 January 2020, La Tour Hassan Palace, Rabat, Morocco

Under Patronage

Supported By:

General Electric GS1

A Medical Device training to learn to about the basic requirements and the upcoming changes to the Medical Device regulations (MDR) in Europe. It will span from pre-market to post-market, it will cover classification of Medical Devices, how to get in compliance with the new MD regulation in Europe, explanation of the major changes to the current Directive. But it will also cover the regulatory side and importance of the supply chain of products. The new terms Clinical Evidence will be explained and the impact to a safe product as well hot topics like biocompatibility, sterilization , borderline products, risk management will be presented and discussed.


  • You will learn about best practice to implementation of the MDR regulation
  • You will be able to discuss your MDR challenges with experts with profound knowledge from the appropriate area
  • You will attend a compact (2 days) training program

Target Audience:

Local regulators in the field of pre-and post-market controls
MedTech industry, MDR manufacturers, regulatory affairs managers, distributors, importers.


La Tour Hassan Palace, Rabat, Morocco


1840 AED for participants



Gwennaelle Even

Deputy, Division for medical devices, cosmetics and invitro
National Medical Agency France

Laurence Matheron


Sophie Dubuc

Non-Clinical Assessor
National Medical, Agency France

Geraldine Lissalde-Bonnet

Director Public Policy
GS1, Global Office

Salma Salim

Regulatory, Affairs Manager

Alexandre Girond

Director, Quality Medical
Device Emerging Markets, J&J

Philip Malca

Global Regulatory Affairs Director
GE Healthcare