Join the American Herbal Products Association (APHA) for a webinar series on FDA Inspection Trends, cGMP Compliance Issues, and Responding to an FDA 483.
Experts will provide an update on FDA inspections, emerging cGMP compliance issues, strategies for responding to an FDA 483 and answers to your specific questions.
This webinar is designed to help businesses in the dietary supplement industry understand the elements of current Good Manufacturing Practice regulations (21 CFR 111) that have been the primary focus of recent FDA inspections. This knowledge will assist business in allocating and directing their compliance resources.
This two-part webinar will provide data on recent FDA inspections, an overview of emerging compliance issues and strategies for responding to an FDA 483 in order to avoid an FDA Warning Letter.
Topics Will Include:
Part 1: November 30
Veteran industry legal experts will provide an insider's view of the current cGMP enforcement landscape and strategies for compliance. AHPA staff will offer a detailed analysis of the association's repository of inspection data, which includes actual FDA 483 inspection reports, observation forms, and establishment inspection reports (EIRs).
A 20-30-minute Q&A session will answer attendees specific questions.
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