Process validation for medical device manufacturers

Process validation for medical device manufacturers

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Process validation for medical device manufacturers
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This video provides regulatory/quality professionals, manufacturing engineers, and process development engineers with the knowledge and skills necessary to meet the process validation requirements of the FDA's Quality System Regulation, ISO 13485, and the GHTF Validation Guideline N99-10, while providing information on how to implement an effective validation program.

For more information contact –

Organization: NetZealous BDA GlobalCompliancePanel
Website: http://www.globalcompliancepanel.com/
Email: [email protected]

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