MDR2020@nov18

MDR Compliance: Get ready for 2020

Join us to prepare survival of the new Medical Device Regulation (MDR): 

  • Key Impacts of the Medical Device Regulation | Mr Erik Poulsen
  • Clinical Evaluation - the Mandatory Requirements of MDR | Mr Kim Rochat
  • Post-Market Surveillance - What to Implement | Mr Erik Poulsen
  • Changes in Software - What to Prepare for a Successful CE Marking | Mr Kim Rochat

4 x 20 minutes presentations illustrated with real cases followed by Q&A

 

The event is co-arranged by Medidee, MedTech Innovation and DTU

 

 

 

1 November 2018

15:00-17:00

Meeting Center at DTU, Room S08

MedTech Innovation - Anker Engelunds Vej 1 - 2800 - Kgs. Lyngby - 51251016 - anryl@dtu.dk