Handling OOS Test Results and Completing Robust Investigations - Webinar

  • ID: 3734847
  • Webinar
  • 60 Minutes
  • Pathwise
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This webinar is designed to provide sound training on how to recognize and investigate atypical or out of specification results, using approaches which have been recommended by regulatory authorities, performing appropriate investigations.

Learning Objectives:

- Learn the responsibilities of Analysts and Supervisors
- Listen to what the FDA looks for in terms of Human Errors
- Describe when a Full Investigation should be triggered
- Describe the frequency for Re-testing and Re-sampling
- Learn how to implement the corrective and preventive action plans (CAPA)
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Danielle DeLucy
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