Corrective and Preventive Actions (CAPA)
Conduct root cause analysis of non-conformities to prevent the occurrence and take corrective action. It is a part of good manufacturing practice (GMP) to control unstable trends in product and process monitoring.
Manage end-to-end incident investigations
Identify root causes and incident trends
Identify potential sources of non-conformities
Design Corrective and Preventive Action Plans
Monitor multiple corrective actions plans