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How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare

10 August 2011, Wilmington, United States


Introduction
This webinar will provide valuable assistance to all companies that market in the U.S., since they are by definition subject to FDA regulation, in the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields.
Venue
online training webinar

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

Organised by
globalcompliancepanel
Contact information
Mr webinar web
United States of America
Contact us by email

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