Avoiding 483 Warning Letters & Remediation if you get one - Webinar By GlobalCompliancePanel 2012
08 Aug 2012
Webinar
Key Topics
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
Who should Attend
IT Management, Project Managers, Quality Managers, Business Process Owners, GxP, Quality Engineers and Consultants.
Past Events
Avoiding 483 Warning Letters & Remediation if you get one - Webinar By GlobalCompliancePanel 2012 - 08 Aug 2012, Webinar (31872)
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Important
Please, check "Avoiding 483 Warning Letters & Remediation if you get one - Webinar By GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements
