SFL’s Head of Combination Products Theresa Jeary and Head of Medical Devices Karin Schulze are providing training at the Medtech & Pharma Platform (MPP) course entitled “Overview of Medical Devices Regulation (MDR) and Impacts for Medtech and Pharmaceutical Industry” (20^th February 2020, Basel). The course provides an overview of the MDR’s regulatory system and examines the consequences of the full implementation of the MDR coming into effect on 26^th May 2020, including new classification and quality management requirements, for medical devices and complex combined devices that utilize medtech with pharma and software components.

SFL’s experienced medical device and combination products teams can support your various MDR implementation projects by performing MDR gap analyses, proposing effective strategies to achieve MDR compliance, and providing hands-on support with all aspects of MDR implementation. Contact us to discuss your projects.