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2021 - Validation Master Plan - The Unwritten Requirements
Date2021-07-13
Deadline2021-07-03
VenueOnline event, USA - United States 
KeywordsValidation master plan; Validation master plan fda; CGMP deficiencies
Topics/Call fo Papers
Verification or Validation - Recent regulatory expectations
The Master Validation Plan
The Individual V&V Plan
Product V&V versus Process / Equipment V&V
When / How to Use DQ, IQ, OQ, PQ, ASTM E2500 Equivalents
Using the Risk Management tools of ISO 14971 and ICH Q9
The 11 Elements of the Software VT&V "Model"
Key recent compliance problems
The Master Validation Plan
The Individual V&V Plan
Product V&V versus Process / Equipment V&V
When / How to Use DQ, IQ, OQ, PQ, ASTM E2500 Equivalents
Using the Risk Management tools of ISO 14971 and ICH Q9
The 11 Elements of the Software VT&V "Model"
Key recent compliance problems
Other CFPs
- On the Alert: Software License Audit Readiness
- FDA Modernization and Restructuring of the SDLC for Computer System Validation (CSV) and Compliance
- Investigation of Out-of-Specification Test Results
- Human Error Reduction in GMP Manufacturing
- Complaint Management: Best Practices to Assure Regulatory Compliance and Customer Retention
Last modified: 2021-06-28 16:39:38