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Overview of Emergo Group Medical Device Regulatory Consultants
Emergo Group helps medical device and IVD manufacturers obtain regulatory approval for their products in the USA, Canada, Mexico, Brazil, Europe, Russia, Japan, China, Korea, India and Australia. Services include US FDA 510(k) submissions, CE Marking for Europe, GMP/ISO 13485 quality system implementation, in-country representation and distribution consulting. Offices located worldwide.
|Category of expertise:||
Management Consulting ,
|Primary location:||United States, United States|
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