Dr. Karin Schulze, Head of Medical Devices & Combination Products at SFL, will meet with Swiss Medtech’s SIT discussion group on the 18^th of January in Zurich. The group will discuss future responsibilities of stakeholders under the new Medical Devices and In Vitro Diagnostics Regulations (MDR and IVDR), with special focus on data provision requirements for the industry. Karin will be happy to discuss the impact of the upcoming Regulations with stakeholders in the medtech field.