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FDA Guidelines for CAPA
As early as 1999, the Federal Drug Administration (FDA), began providing CAPA guidelines and started to actively enforce CAPA requirements as part of its Quality System Inspection Technique (QSIT) initiative. Corrective action is defined as an action undertaken to eliminate the cause of an existing non-conformity, defect or other undesirable situation to prevent recurrence. Preventive action is defined as an action undertaken to eliminate the cause of a potential non-conformity, defect or other undesirable situation to prevent an occurrence. Four key words are different in the two definitions: existing and potential, and recurrence and occurrence.

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