sitem-insel AG

M4 - EU Medical Device Regulations Part C

Module leaders: Dr. Jürgen Berndt, Independent Consultant
Beat U. Steffen, confinis ag
Szymon Kurdyn, DQS Medizinprodukte GmbH

Date and Credits

Start: 19.04.2021

Duration: 10 Weeks


Module 4 is comprised of three submodules covering the regulation of labelling and instructions for use, conformity assessment and product registration, and post market surveillance and post market clinical follow-up.