SFL to speak at the Swiss Medtech IVDR&MDR Conference
SFL’s Head of Regulatory Affairs and Medical Devices Karin Schulze will present the new Medical Devices Regulation (MDR) and new compliance guidelines for product materials and hazardous substances at the 3rd national Swiss Medtech IVDR&MDR conference (4th of April 2019, Bern). The event’s program will focus on the status of the new MDR’s implementation and its effects on Switzerland. SFL’s CEO Shayesteh Fürst-Ladani, and Senior Public Affairs Manager Christine Kantsperger representing the Secretariat of the MedTech and Pharma Platform (MPP), will also attend the event. SFL has extensive experience in the field of Medical Devices and particularly Combination Products (i.e. products that comprise both an active drug component and physical device component).
Karin, Shayesteh and Christine would be happy to discuss your projects and areas to support your medical devices and combination products, from strategic advice on development, clinical evaluation, to QMS, to CE-marking and post-marketing maintenance.