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The FDA Inspection Process: From SOP to 483 - Webinar By GlobalCompliancePanel

20 September 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,, de, Suite 1200, Wilmington, 19801, United States

Organised by
global compliance panel
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