News

22.03.18

Mini symposium: Clinical evaluation and market observation according to MDR

Regulation (EU) 2017/745 on medical devices (MDR)
has been in force since May 2017. Although the interpretation of
many requirements remain controversial and
there are no additional legal acts so far, the transitional period
progresses and it should be implemented concrete action now. It's about to use the remaining time effectively and to implement the requirements into practicable procedures. Therefore, we have selected outstanding topics for you:

  • The transition from MDD to MDR: a strategical challenge
  • PMCF and anti-corruption law - which possibilties are still given?
  • Future market and product observation of medical devices after placing on the market - from planning to PSUR. What should already be prepared?
  • Clinical trials and PMCF - sneaking out is not an option (anymore)

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

 

Detailed information (German only) can be found here.

 

Date: June 12, 2018 in Reutlingen                  

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

Event location: TTR Technologieparks Tübingen-Reutlingen GmbH, Gerhard-Kindler-Str. 6, 72770 Reutlingen

 

Date: June 13, 2018 in Stuttgart                           

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

Event location: VOELKER & Partner Rechtsanwälte Wirtschaftsprüfer Steuerberater mbB, Tübingen STraße 26 (Im Gerber), 70178 Stuttgart

 

Attendance fee: 90,00 € (excl. 19 % VAT) each person

Registration until May 25, 2018

via E-Mail: info@schrack-partner.eu

Fax: 07121 / 51068-0

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

Please provide details on date and venue.