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Master Verification & Validation Planning under U.S. FDA CGMP, ICH Q-series and ISO 13485-14971 Requirements - Webinar By GlobalCompliancePanel

21 March 2012, Wilmington, United States


Introduction
FDA Warning Letters and recent high-profile recalls indicate major cGMP deficiencies in many companies.

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Venue
Online Training

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

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Organised by
GlobalCompliancePanel
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