After our two MDR webinars last October and December, it's time for the third webinar. The upcoming webinar will focus on the changes in Classification and Conformity Assessment Routes in the MDR compared to the Medical Device Directive (MDD). Subscribe now and learn more!
On January 23, DEKRA’s MDR expert and President of Team NB Guy Buijzen and Principal Certification Manager Alex Laan will address, amongst others:
- The main differences between the regulatory classification of medical devices under Medical Device Directive 93/42/EEC and the EU Regulation 2017/745 (MDR)
- New elements in the conformity assessment of the medical devices under the EU Regulation 2017/745 (MDR)
- Regulatory strategies for medical device manufacturers to transition to the EU Regulation 2017/745 (MDR)
The "Expert Sessions MDR" is a series of webinars that sheds light on the most important aspects or developments around the new regulation. In the first session, broadcasted on October 23, we gave an update of the most important developments. The webinar on December 19, 2017 focused on Clinical Evaluation Requirements.
We are looking forward to welcoming you! Please click the 'Subscribe' button to join us. Not able to watch live? Subscribe and receive the link after the webinar to watch the on demand version.
For your convenience we are additionally organizing an IVDR webinar on February 15. Secure your spot for this webinar also and subscribe now to learn about the current status of the transition to IVDR. Please note that we will also organize various other webinars in 2018.