Webinar "The New In Vitro Diagnostic Regulation"

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?


  • Get an overview of the schedule of the transition
  • What are some of the changes/new developments with regard to classification, conformity assessment and performance evaluation?
  • As an IVD manufacturer, what can you do already today to best prepare yourself for the new regulation?

Registration to our webinar

In return for attending on our webinar, we only request your contact details and your consent  to receive in the future regular updates from TÜV Rheinland about services and news via e-mail.

You will receive a confirmation of your registration by e-mail.
 After the event, we will make the presentation available to you as a download. If you have any questions or require further information, please do not hesitate to contact us: messe@de.tuv.com