SFL to speak in Swiss MDR/IVDR Forum
How can ISO 13485 be correctly implemented under the upcoming Medical Devices and In Vitro Diagnostics Regulations (MDR and IVDR)? Karin Schulze, SFL’s Head of Medical Devices & Combination Products, will discuss this topic at the Swiss MDR/IVDR Forum, organized by Swiss Medtech and the Swiss Institute for Translational and Entrepreneurial Medicine (sitem-insel). The event, entitled “Partnership for success: jointly solving the challenges of MDR/IVDR” will take place in Bern on the 16th of April 2018 and feature presentations and podium discussions from relevant Swiss stakeholders.
SFL can support you to ensure business continuity during the transition period for the MDR and IVDR. Contact us to arrange a meeting with Karin during the Forum.