Avoiding 483 Warning Letters & Remediation if you get one - Webinar By GlobalCompliancePanel 2012

  • 08 Aug 2012
  • Webinar

Description

Avoiding 483 Warning Letters & Remediation if you get one is a webinar that covers topics such as:

  • Causes of Form 483 / Warning Letter
  • FDA Inspections - background
  • Best Practices for Responding to 483
  • Some recent results of companies failing to respond appropriately
  • What to do if the responses fail
  • Best Practices for Responding to Warning Letter

Avoiding 483 Warning Letters & Remediation if you get one brings together IT Management, Project Managers, Quality Managers, Business Process Owners, GxP, Quality Engineers and Consultants.

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Important

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Event Categories

Health & Medicine: Medical device, Pharma
Industry: Food & Beverages

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