Workshop on the new Medical Device Directive 

Published by HTAde on

Less than two years before the new European Medical Device Directive (MDR) comes into force,, together with the DGSMP and the Network for Evidence-based Medicine, has drawn an interim conclusion to the discussion on the evaluation of examination and treatment methods with medical devices. For this purpose a workshop was held in Dresden on 9/12/2018. The presentations can be found below.

Lecture slides

  • Grundzüge und Einschätzung der MDR aus HTA-Sicht (M. Perleth)
  • Verbindung zwischen HTA und MDR – EUnetHTA Task Force / Roadmap (P. Schnell-Inderst)
  • Forschungslücken / Forschungsbedarf hinsichtlich HTA und Medizinprodukten (D. Lühmann)
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