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.

Key Features:
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
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