Process Validation for Medical Device Manufacturers
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- เผยแพร่เมื่อ 5 มิ.ย. 2016
- This Video provides regulatory/quality professionals, manufacturing engineers, and process development engineers with the knowledge and skills needed to comply with the process validation requirements of the FDA's Quality System Regulation, ISO 13485 and the GHTF Validation guidance N99-10 while offering information on how to implement an effective validation program.
For More Information Contact -
Organization: NetZealous BDA GlobalCompliancePanel
Website: www.globalcompliancepanel.com/
Email: support@globalcompliancepanel.com
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This is a great presentation
Very informative. Thank you!
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Very good