Mini symposium: News on the implementation of the MDR

The implementation of Regulation (EU) 2017/745 on medical devices (MDR) continues to progress and half of the transition period until final mandatory application has already elapsed. During this event, you will learn about the current status of the interpretations as well as information on efficient implementation within the company.  

The following topics await you this time:

- The transition from MDD to MDR: What needs to be considered during planning? – An evaluation from the point of view of a Notified Body
- Responsibilities and liability according to the new MDR
- How do QM systems become fit for MDR?
- PSUR (Periodic Safety Update Report)


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

Detailed information can be found here.



Date: November 27, 2018 in Reutlingen

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


Date: November 28, 2018 in Stuttgart

Time: 5:00 - 8:00 p.m.
Venue: 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 November16, 2018
By e-mail to:

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