Mini-Symposium: news on the MDR - the countdown is on!

According to a recent survey by the German Chambers of Industry and Commerce and the Spectaris industry association, almost 80% of medical technology companies expect to encounter considerable difficulties in introducing innovative products onto the market in the future. A major reason for this concern is the introduction plan for the new EU Medical Device Regulation (MDR), whose increasing requirements are threatening small and medium-sized suppliers in particular. Even though many supplementary legal acts are still missing and thus many uncertainties remain, it is now all the more important to take the necessary measures in the company to prepare for the MDR.

The following topics awaits you this time:

- MDR - The greatest challenges for manufacturers and Notified Bodies
- Liability law and commercial law problems under the MDR
- Requirements of the MDR for QM systems: Where do we stand?
- Clinical investigation from the point of view of the MDR

Afterwards there will be enough time for discussion and for your questions on these central topics.


Detailed information can be found here.


May 07, 2019 in Reutlingen

5:00 - 8:00 p.m.
TTR Technologiepark Tübingen-Reutlingen GmbH, Gerhard-Kindler-Straße 6, 72770 Reutlingen


May 08, 2019 in Stuttgart

5:00 - 8:00 p.m.
VOELKER & Partner Rechtanwälte Wirtschaftsprüfer Steuerberater mbB, Tübinger Straße 26 (Im Gerber), 70178 Stuttgart


A contribution towards expenses of € 90.00 per person plus 19% statutory value-added tax must be paid for participation.
Registration until April 29, 2019
By e-mail to:

Please be sure to include the date and venue with your registration.