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Recent Major Industry CGMP Failures and How to Avoid Them

10 August 2011, Wilmington, United States


Introduction
U. S. FDA-regulated companies are responsible for understanding current Good Manufacturing Practices (CGMPs) as defined in the Code of Federal Regulations ( 21 CFR Part 111, 210/211, and 820). They are then required to translate those regulations into procedures and work instructions.

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Venue
online training webinar

online training webinar, 1000 N West Street Suite,, Suite 1200, Wilmington, 19801, United States

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Organised by
globalcompliancepanel
Contact information
Mr webinar web
08004479407
Contact us by email

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