The impact of the new MDR on clinical affairs
Thursday 22 June 2017 - Zurich



During this half-day session genae will provide insight to the new Medical Device Regulation (MDR) and the changes your organization will face. 

SCHEDULE:  
  • 1.30-2.00 PM: welcome
  • 2.00-4.00 PM: presentation (part I)
  • 4.00-4.30 PM: break
  • 4.30-6.00 PM: presentation (part II)
SPEAKERS:
  • Zuzanna Kwade, PhD - Sr. Clinical Safety Manager
  • Mieke Roelants, PhD - Sr. Regulatory Affairs Manager
LOCATION: Holiday Inn Zürich Messe, Wallisellenstrasse 48, 8050 Zürich

Sign up for this must attend event and get prepared for the new MDR!

 
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