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Last updated on April 19, 2014 at 18:42 EDT

Latest GPMG Stories

2013-02-28 08:29:38

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. GARDNER, Mass., Feb. 28, 2013 /PRNewswire/ -- Global Pacific Manufacturing Group LLC's (www.gpacmfg.com), quality system product helps specification developers be ISO 13485 Certified and FDA QSR compliant in 3 months or less. The GPMG base...

2013-02-27 08:29:26

GPMG, a medical device consulting firm, unveiled a new product to help Initial Importers of medical devices comply with FDA regulations. The design of the system allows for immediate implementation and fits varying organizational structures. GARDNER, Mass., Feb. 27, 2013 /PRNewswire/ -- Global Pacific Manufacturing Group LLC (www.gpacmfg.com), has developed a practical and cost-effective quality system to help the thousands of current and future Initial Importers be FDA compliant. A...