The new IVD Regulation 2017/746 (IVDR) will fundamentally change the regulatory procedure for the entry of in vitro diagnostic devices (IVD) to the EU market. Since the transition of products and processes with regard to the new regulation will be very time-consuming and complex, we recommend to prepare early and to coordinate with a Notified Body.
Our webinar "The New In Vitro Diagnostic Regulation" will give you a comprehensive overview of the changes that await manufacturers of in vitro diagnostic medical devices.
This one-hour webinar is specifically designed for IVD professionals in the areas of quality management and regulatory affairs who have a basic knowledge of the IVDR.
We will provide you with comprehensive information about the requirements of the new IVD regulation.
Prepare early and register for our webinar on 27 June 2019, 10 to 11 am or 3 to 4 pm (CEST).
We're looking forward to seeing you in our webinar.
What do you expect?
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