Events

Online Workshop: Basics of Regulatory Affairs in MedTech

This training provides you with the basics of regulatory affairs in MedTech with the focus on MDR and IVDR (Medical Devices and In-Vitro Diagnostic Medical Devices Regulation). Get an overview of the regulatory lands- cape, hear about the basic concepts and principles and get insights into the necessary steps but also pitfalls when bringing a MedTech product to the market. Discuss with the experts.

More information here.