SFL’s Head Regulatory Affairs & Medical Devices, Karin Schulze, will attend the upcoming SAQ medical devices expert group meeting (Fachgruppe Medizinprodukte) on the Medical Device Single Audit Program (MDSAP). The conference, taking place in Olten on 13 September 2018, will focus on an introduction to the MDSAP, the notified body’s perspective and insights from past experiences with the Program in order to obtain a successful CE marking certification.

As the former head of a notified body, Karin and SFL’s Quality Assurance department support clients in preparing for notified body audits and in implementing corrective actions. Please contact us to arrange a meeting with Karin during the event.