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Europe: Medical Devices - The Notified Body Consultation Procedure, Part 1

27/9/2011

Manufacturers of medical devices incorporating ancillary substances should have a clear understanding of the consultation procedure that their Notified Body will have to follow. 

 

Part 1 of this article discusses the regulatory requirements and important guidance documents.  More...

 

Author: Greer Deal, Director of Global Regulatory Services (GRS)

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