Understanding Investigations, Root Causes and Implementing an Effective CAPA System

Topic: Biopharmaceuticals, Manufacturing

Issues get reported on daily basis by the functional areas some of these issues are minor and some are serious enough to warrant a proper investigation.

This session will cover – What are serious quality issues, how are these reported and managed, leading to CAPA management (a 5 step process covering investigation of the issue, root cause, CAPA actions and effective checks).

An example of handling a serious quality issue will be shared during the webinar.

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