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Clinical Evaluation Requirements under European Medical Device Regulation, Impact on Businesses, and Brussels Update

 Maria E. Donawa M.D.
  22nd-Feb-2018
Description: Clinical Evaluation Requirements under European Medical Device Regulation, Impact on Businesses, and Brussels Update.
Views: 1136
Domain: Medical
Category: Implants
Contributing Organization: MassMEDIC
 ‐ More of their Presentations
SEMICONDUCTOR ANALYTICS
Contents:
Clinical Evaluation Requirements under European
Medical Device Regulation, Impact on Businesses,
and Brussels Update
MassMEDIC Webinar
18 January 2018, 12:00 - 13:00 EST
Maria E. Donawa, M.D.
President
Donawa Lifescience Consulting Srl
18 Jan 2018

TOPICS


New clinical evaluation requirements under Medical Device
Regulation (MDR)



EU Guidelines on Clinical Evaluation (MEDDEV 2.7/1 ... See more

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