An organization's corrective action preventive action (CAPA) process is central to all control points. Corrective actions are intended to determine the cause of nonconformances that have been detected, while preventive actions are the plan put in place to stop the problem from happening again in the future.
Replacing a paper-based CAPA process with an electronic system is challenging, not to mention connecting it with change control, training and other quality systems. The resources below explain what to look for in an electronic system and how an automated corrective action preventive action system clearly brings great benefits, not only in terms of cost savings but also in terms of product safety and effectiveness.
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