SFL’s Head of Medical Devices, Karin Schulze, is presenting on “What are the duties of a Legal Manufacturer, how are incidents managed, what should be reported, FSCA and FSN” (28 January 2020, Muttenz). The lecture is part of the continuing education course on clinical, regulatory and quality affairs for medical devices and in-vitro diagnostics (CAS CARAQA) offered by the School of Life Sciences at the University of Applied Sciences and Arts Northwestern Switzerland (FHNW).

Karin, an expert in medical devices and former head of a Notified Body, regularly provides lectures and training. You can hear about this topic and more by registering to attend the next training she will provide for the Medtech & Pharma Platform on the “Medical Devices Regulation and Impacts for Medtech and Pharmaceutical Industry” on 20^th February, 2020.

SFL has extensive experience in the field of Medical Devices and a dedicated Combination Products Team focused on these complex products comprising both a pharmacologically active drug component and physical device component. Contact us to arrange a call with Karin to discuss your projects and how SFL can support your medical devices and combination products, from strategic advice on development, clinical evaluation, to QMS, to CE-marking and post-marketing maintenance.