Minisymposium: The new European Medical Device Directive

The new European Regulatory of medical device certification is published now. Medical device manufacturers should prepare for the expected changes in order to initiate the right steps at the right time during the transition period.

Our symposium will provide an overview of regulatory changes, especially those associated with far-reaching consequences. We will inform you about the current status of the practical implementation of these reforms and address the subject from a legal perspective as well as from the point of view of a notified body. 

The symposium will also focus on changes regarding the clinical evaluation of medical devices and quality management systems as well as new legal risks.

After that, there will be sufficient time for discussion and your questions on this important topic.


Detailed information (German only) can be found here.


Date: October 04, 2017                           

Time: 5:00 p.m. - 8:00 p.m.            

Organizer: Schrack & Partner                   

Event location: in Dominohaus at VOELKER & Partner - Rechtsanwälte Wirtschaftsprüfer - Steuerberater mbB, Am Echazufer 24, 72764 Reutlingen


Date: October 05, 2017                           

Time: 5:00 p.m. - 8:00 p.m.           

Organizer: DEKRA Certification GmbH            

Event location: Intercity Hotel Frankfurt Airport, Am Luftbrückendenkmal 1, 60549 Frankfurt/Main


Attendance fee: 70,00 € (excl. 19 % VAT) per person

Registration until September 25, 2017

via E-Mail:

Fax: 07121 / 5106899

Postal: Schrack & Partner / Gerhard-Kindler-Str. 6 / 72770 Reutlingen

Please provide details on date and venue.