Corrective and Preventive Action (CAPA) Procedure for GMP
GMPSOP
MARCH 17, 2023
By definition, corrective actions are required to eliminate the causes of an existing nonconformity, defect, or other undesirable situation. In a packaging line, a printer was used to imprint manufacturing and expiry dates on a batch of empty cartons which will be used to fill tablet strips. QA Inspector found no defect on those.
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