describe the image A corrective action procedure is not reworking or remaking an item to bring it back into specification. Patching up a mistake doesn't address what made it happen in the first place and it won't prevent a recurrence.

CAPA Inspectional Guidelines and Flow Chart

Why is a Corrective Action Preventive Action (CAPA) System Important?

The methods for dealing with corrective and preventive actions require a high level of accuracy and flexibility. Rigorous regulatory and traceability requirements exist in industries such as life sciences or any other manufacturing operation.

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Implementing a corrective preventive action (CAPA) system should be an important part of any corporate quality system, regardless of industry.


Download CAPA Guidelines