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Technical Documentation and Medical Device Regulation

 Julianne Bobela PhD, Benjamin Frisch PhD, Kim Rochat, Michael Maier
  24th-Aug-2018
Description: Before placing a medical device on the European market, manufacturers need to produce technical documentation providing evidence of conformity with the relevant legislation.
Views: 5609
Domain: Medical
Category: Implants
Contributing Organization: MEDIDEE SERVICES SA
 ‐ More of their Presentations
Contents:
Technical Documentation and Medical
Device Regulation
A Guide for Manufacturers to Ensure Technical Documentation
Complies with EU Medical Device Regulation 2017/745
Dr Julianne Bobela, Project Associate; Dr Benjamin Frisch, Senior Associate; Kim Rochat,
Senior Partner; and Michael Maier, Senior Partner; all at Medidee Services SA

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Introduction1
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