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Webinar: FDA Inspection Trends, cGMP Compliance Issues and Responding to an FDA 483

Nov. 30 (FDA Inspections and Emerging cGMP Compliance Issues) -- Dec. 14 (Q&A and Responding to an FDA 483)

This two-part webinar will provide an update on the elements of current Good Manufacturing Practice (cGMP) regulations (21 CFR 111) that have been the primary focus of recent FDA inspections. Experts will also provide strategies to respond to an FDA  483 in order to avoid a warning letter.


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