戻る Agenda
MDR Implementation – Status Quo
Session Chair(s)
Shayesteh Fürst-Ladani, MBA, MS
CEO
SFL Regulatory Affairs & Scientific Communication, Switzerland
This session will provide an overview of the Implementation of Medical Devices Regulation (MDR) from competent authority, industry and notified body perspectives.
Speaker(s)
Clinical Investigations with Medical Devices
Stefan Strasser, MD
AGES, Austria
Head of Clinical Trials, Institute Surveillance
Lessons learnt to certify QMS system and product against the EU MDR
Mike Wallenstein, MSC
Novartis , Switzerland
Global Head MDR Implementation and DD&C Compliane