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  • Are You Prepared For The New EU Medical Device Regulation? | Webinar | 9 November 2017
09. 11.2017

Are You Prepared For The New EU Medical Device Regulation? | Webinar | 9 November 2017

The new EU Medical Device Regulation (MDR) was officially passed in May 2017 and manufacturers now have until 2020, to be fully compliant with all changes set forth within the new regulation. View this webinar to better understand the changes that clinical affairs teams should prepare for now to be successful under the new regulation.

Discussion points during this 30 min. webinar include:

  • Impact on the clinical strategy
  • Portfolio analysis
  • Post-market clinical follow-up 
  • Changes to Notified Bodies
  • Clinical evaluation and CER
  • Transparency of information