This webinar will provide valuable guidance to regulated companies in development, implementation, or refinement of their manufacturing process verification and validation programs. It will evaluate validation practices that are more in agreement with ICH Q7 and Q8 than previously accepted validation methods, and will provide thought-provoking questions for FDA-regulated companies.
Process Verification and Validation to Meet U.S. FDA Requirements - Webinar By GlobalCompliancePanel
25 April 2012, Wilmington, United States
Introduction
Venue
OnlineTraining
OnlineTraining, 1000 N West Street,, Delaware, Suite 1200, Wilmington, 19801, United States
Useful links
Organised by
GlobalCompliancePanel
Contact information
Related events
TAC 2025 - 60th Anniversary Conference
14 April 2025 09:00 - 16 April 2025 17:00, Guildford, United Kingdom
What's in that Perfume? - The Chemistry behind an iconic Christmas gift
3 December 2024 18:00-20:00, London, United Kingdom
Chemistry Teaching in Practice
9 January 2025 09:30-16:00, Oxford, United Kingdom
Joint SoBRA / UUÂãÁÄÖ±²¥ Winter Conference 2024 Current Issues in Contaminated Land Risk Assessment
10 December 2024 09:45-18:00, London, United Kingdom
Search
Advertisement
Spotlight
Explore
Membership
