SFL will speak at SAQ’s medical products expert group meeting
SFL’s Head Regulatory Affairs, Karin Schulze, will speak at the upcoming SAQ’s medical products expert group meeting (Fachgruppe Medizinprodukte) on the Medical Devices Regulation (MDR). The event, taking place in Olten on the 14th of June, features presentations on the major changes and challenges faced by the medical device industry. Karin is a member of the expert group and will present the key elements related to post-market surveillance (PMS) and post-market clinical follow-up (PMCF).
SFL’s Regulatory Affairs department is supporting clients in the transition from the Medical Devices Directive (MDD) to the MDR. Please contact us to arrange a meeting with Karin during the event.