A robust Corrective and Preventive Action (CAPA) program is of the utmost importance to a medical device manufacturer.

A system that identifies and eliminates nonconformances and potential nonconformances enables both regulatory compliance and cost savings.

This video shows the importance, requirements, and elements of a CAPA program, as well as describing the uses of CAPA data. Additionally, the application of risk management to a CAPA program will be reviewed, and a specific risk management system explained.


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Organization: NetZealous BDA GlobalCompliancePanel
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Email: support@globalcompliancepanel.com

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