Compliance Trainings

Webinar on IQ, OQ, PQ in the Verification and Validation Process

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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:
Webinar
Date:
Oct. 18, 2016
Venue:
Online
Location:
Online

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