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.
The FDA Inspection Process: From SOP to 483 - Webinar By GlobalCompliancePanel
20 September 2011, Wilmington, United States
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online training webinar
online training webinar, 1000 N West Street,, de, Suite 1200, Wilmington, 19801, United States
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global compliance panel
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