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Emergo Group Inc.

Specializes in medical device regulatory affairs, product compliance, and quality system implementation

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Medical, device, regulatory affairs, CE Mark, medical device, CE Marking, ISO 13485, ISO 13485 2003, FDA compliance, FDAGMP, FDA cGMP, 510(k), 510k, 510 k, Authorized Representative, ISO 14971, ISO 14971 2000, risk management, consultants, Medical device directive, CE Marking Directive, US agent,...

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Telephone 1.512.327.9997Email contact emergogroup.comOnline www.emergogroup.com
CE Mark CE MarkingAuthorized RepresentativeISO 13485 Implementation
Medical Distributor SearchALL services for Europe...
FDA Agent RepresentationGMP ImplementationDevice Classification
Clinical Trial ConsultingMedical Distributor SearchALL services for Australia...
ISO 13485 ConsultingCMDR ConsultingMDEL or MDL License
Technical File Preparati...


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