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What to Expect and How to Prepare for FDA Inspections

Wednesday, June 22, 2011
Online Training Webinars
Wilmington, United States

Event Type: Exhibitions


As recent headlines demonstrate, non-compliance with US Food & Drug Administration US FDA laws and regulations could cost your firm millions.

In addition to significant revenue losses, violative US FDA inspections may also lead to injunctions, consent decrees, warning letters, FDA 483 's Notice of Inspectional Observations, product non-approvals, import detentions, recalls, criminal investigations and prosecutions, seizures, compliance problems, FDA compliance meetings, and monetary penalties.

FDA's mission is to promote and protect the public health by helping safe and effective products reach the market in a timely way and monitoring products for continued safety after they are in use. One way that the FDA fulfills its mission is through inspections of developers, manufacturers, laboratories, and distributors of regulated products. Inspections ensure a firm is compliant with US Food and Drug Administration Laws and Regulations.

In this FDA cGMP Inspection training learn all the background information and key Techniques needed to guarantee a cost-effective, first-time pass through an FDA inspection - whether for a pharmaceutical product, an active pharmaceutical ingredient (API), a medical Device or a biological production.

This webinar is designed to provide background and insight into the inspection process, as well as practical strategies and tactics that a company must know and implement in order to have the potential to pass an inspection the first time through. The inspection process itself will be analyzed and reviewed in a manner that will allow you to immediately begin effective strategizing on how to pass the inspection.


Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00

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