Project Management for Computer Systems Validation - Webinar By GlobalCompliancePanel 2012

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.