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FDA specification developers Remove


June 2013
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Page 1

FDA specification developers Latest News

 



GPMG Product Helps Medical Device Specification Developers be FDA and ISO 13485 Compliant
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.





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