29. 11.2018

Are You Prepared For The EU Medical Device Regulation? | Webinar | 29 November 2018

The EU Medical Device Regulation (MDR) was officially passed in May 2017 and manufacturers have until 2020, to be fully compliant with all changes set forth within the new regulation. View this 30 min. webinar to better understand the changes that clinical 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
  • Post-market clinical follow-up 
  • Changes to Notified Bodies
  • Clinical evaluation and CER
  • Transparency of information