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By Global Pacific Manufacturing Group LLC
GPMG, a medical device consulting firm, unveiled a quality system product designed for specification developers. The FDA QSR and ISO 13485 compliant system governs all aspects of product development, design transfer, and device master records.
By Stewart Eisenhart
Emergo Group now offers comprehensive clinical trial management and support in Japan through partnership with NTT Data Group.
By Emergo Group, Inc.
Medical device regulatory consulting firm Emergo Group recently surveyed medical device and IVD manufacturers, distributors and industry service providers about the state of their company, international expansion plans and their outlook for 2010.
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