SFL’s Head of Medical Devices provides Medical Devices Regulation (MDR) training focused on combination products
SFL’s Head of Medical Devices Karin Schulze is providing training at the Medtech & Pharma Platform course entitled “Overview of Medical Devices Regulation and Impacts on Combination Products” (29 September 2020, Online). The course provides an overview of the MDR’s regulatory system and the latest updates on the implementation of the MDR. The course will emphasize the implementation requirements to keep processes and portfolios compliant, and products, including Combination Products, on the market when the MDR finally replaces the existing Medical Device Directive (MDD) legislation in May 2021.
SFL’s experienced medical device and combination products team 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. Please contact us to discuss your projects.