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 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.


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Organization: NetZealous BDA GlobalCompliancePanel

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  1. GlobalCompliance Panel
  2. Process Validation for Medical Devices
  3. FDA's Quality System Regulation
  4. how to maintain adequate validation documentation systems
  5. General Principals of Process Validation
  6. GHTF Validation guidance N99-10
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