Webinar on IQ, OQ, PQ in the Verification and Validation Process
This webinar will discuss the Consideration of IQ, OQ, and PQ and their equivalents for processes, equipment (production and test), product, and CGMP e-records / e-signatures.
Areas Covered in the Session : IQ, OQ, and PQ, major components of robust Verification and Validation V&V programs - Regulatory requirements The Master Validation Plan(s) Individual V&V Plans and their execution Product Verification and Validation Process and Equipment V&V; including software QMS V&V and 21 CFR Part 11 When / How to Use DQ, IQ, OQ, PQ, or ASTM E2500 Equivalents The 11 Elements of the FDA`s Software VT&V "Model"
Who Will Benefit: Senior management Middle management Research & Development Engineering Software QA / RA Manufacturing Operators Consultants cGMP instructors All personnel involved in verification and/or validation planning, execution and documentat
- Event Type:
- Oct. 18, 2016