About trainings

The objective of the MPP is to support synergies between the medtech and pharma industries by establishing a forum to exchange knowledge and collaborate in the areas of technology and regulatory policy, while building stakeholder consensus to promote product development and innovation.

To this aim, the MPP dispenses accredited trainings throughout the year in addition to its annual meeting.

Target audience: Professionals and individuals in the medtech and pharma sectors.

Topics: The topics are varied, but broadly cover industry, regulatory and technical developments.

Course leaders: All trainings are given by topic experts.

Upcoming training

In einem Meeting

20 February 2020

Basel, Switzerland

Overview of Medical Devices Regulation and Impacts for Medtech and Pharmaceutical Industry

Special Focus: MDR implementation for medical devices and combination products

Head of Combination Products

Theresa Jeary, SFL

Stephan Affolter, Ypsomed

Regulatory and Quality Intelligence Manager

Karin Schulze, SFL

Head Medical Devices

Juan Martin Carriquiry, Novartis

EU MDR Expert

Past training

In einem Meeting

27 November 2019

Basel, Switzerland

Overview of key requirements for combination and substance based products under MDR

Special Focus: Combination and substance based products - Assessment under the MDR and Key Requirements

Head of Combination Products

Theresa Jeary, SFL

Stephan Affolter, Ypsomed

Head of Quality System & Regulatory Affairs

Karin Schulze, SFL

Head Medical Devices