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November 2014
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fda qsr Press Releases

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By Global Pacific Manufacturing Group LLC
GPMG LLC, a medical device consulting firm, has exceeded sales expectations for its medical device ISO 13485 quality system products.

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 ComplianceOnline
This 90-minute webinar will help you understand the competence and training requirements in the Quality Management Systems for medical devices, especially FDA QSR, ISO 13485, and even ISO 9001.

By ComplianceOnline
This presentation will review the QSR and ISO requirements for document control, and provide a streamlined process for document control.

By Marie Teixeira
QARACC's 2-Day QMS Training course was designed for medical device manufacturers looking to gain a thorough understanding of the quality system compliance requirements for the distribution of medical devices domestically and internationally.



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