In order to proactively address areas of concern to the FDA and other regulators, All units within each pharmaceutical firm should review recent regulatory observations and proactively establish programs or systems to address the regulatory concerns.
FDA 483 Observations in the Laboratory. What went wrong? How can they be avoided? - Webinar By GlobalCompliancePanel
12 January 2011, Wilmington, United States
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Online Training Webinar
Online Training Webinar, 1000 N West Street | Suite 1200, Wilmington, 19801, United States
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