Introduction

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.

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• Further event details More information about the event

Venue

OnlineTraining

OnlineTraining, 1000 N West Street,, Delaware, Suite 1200, Wilmington, 19801, United States

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• Venue information More information about the venue

Organised by

GlobalCompliancePanel

Contact information

Mr webinars web
OnlineTraining, 1000 N West Street, Suite 1200, Wilmington, 19801, United States of America
8004479407
Contact us by email

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