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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
Other CFPs
- How to Go from Pivot Tables to Dashboards Using Excel
- Complaint Handling Requirements (US); Interrelationship with CAPA, Change Control, Adverse Event Reporting, Recalls and Life Cycle Process Activities
- Best Practices for an Effective Cleaning Validation Program
- How to Prepare a Standard Operating Procedure (SOP)?
- You have a BI Positive or Product Sterility Positive - Now What?
Last modified: 2019-10-29 23:29:13