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

Head of Combination Products

Theresa Jeary, SFL

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

27 November 2019

Basel, Switzerland

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

Programme

Registration

Head of Quality System & Regulatory Affairs

Stephan Affolter, Ypsomed

Karin Schulze, SFL

Head Medical Devices

Past training

Head Medical Devices

Karin Schulze, SFL

Overview of Medical Devices Regulation and Impact on Industry

17 June 2019

Basel, Switzerland

Special Focus: Clinical Decision Support Software and Apps under the Regime of the MDR. As software and apps become increasingly important in the medical sector, the training will provide legal and regulatory perspectives on questions related to software as medical devices

Miguel Cárdenas-Moranta, Novartis

Regulatory Associate Director Medical Devices

Programme

Registration

Lead Expert Software Development

Mithun Ratnakumar, Novartis