june, 2021

Event Details
This training provides you with the basics of regulatory affairs in MedTech with a focus on MDR and IVDR (Medical Devices and In-Vitro Diagnostic Medical
Event Details
This training provides you with the basics of regulatory affairs in MedTech with a focus on MDR and IVDR (Medical Devices and In-Vitro Diagnostic Medical Devices Regulation).
Get an overview of the regulatory landscape, 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 Medidee experts about the different Steps to CE marking for Medical Devices; US Market Access for MD and V&V and Technical documentation!
Ready to participate? Register now, it’s free of charge!
Time
June 29 (Tuesday) 10:00 am - July 1 (Thursday) 12:00 pm CEST
Location
Online Event