FDA Compliant Handling of Out-of-Trend Results in Pharmaceutical Quality Control

Описание к видео FDA Compliant Handling of Out-of-Trend Results in Pharmaceutical Quality Control

This webinar will discuss the FDA requirements and guidelines for investigating Out-of-trend (OOT) results in the pharmaceutical laboratory. It will also cover FDA compliant documentation of OOS, OOT, failure investigations, root causes and CAPA.

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