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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.
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.
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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