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Adverse Event Reporting for Dietary Supplements and OTC Drugs - Webinar By GlobalCompliancePanel

28 June 2011, Wilmington, United States


Introduction
Since passage of the Dietary Supplement & Nonprescription Drug Consumer Protection Act in Dec. 2007, FDA requires reporting of serious adverse events for dietary supplements and OTC drugs.

Manufacturers and importers of products in these categories often have questions about what constitutes a serious adverse event and about Adverse Event reporting requirements that this Webinar will be able to answer.

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Venue
Online Training Webinars

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

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Organised by
GlobalCompliancePanel
Contact information
Mr David Ross
Wilmington, 19801, United States of America
800-447-9407
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