Remove 2005 Remove Labelling Remove Pharmaceutical Manufacturing
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Corrective and Preventive Action (CAPA) Procedure for GMP

GMPSOP

ISO 9000:2005 Sec. – Status control: implementing status labels to clearly identify workflow status such as issues, returns, rejects and reworks of components to prevent mix ups. Basically, you should take all sorts of preventive measures as directed by the outcomes of the investigation. What is corrective and preventive action?