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2019 - Validation Master Plan - The Unwritten Requirements
Date2019-11-20
Deadline2019-11-20
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
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Last modified: 2019-07-06 21:22:30