Sparta Systems, Inc.

In today’s increasingly regulated business environment, a pharmaceutical company’s need to investigate and track quality related events remains a crucial factor in the day-to-day manufacturing operations.

Having a corrective action/preventive action (CAPA) system is a critical component of a good manufacturing practice (GMP) quality system. An effective CAPA system focuses on structured, repeatable investigations of quality events and product non-conformances to first determine the root causes of these events so that issues can be resolved and action can be taken to prevent future occurrences.

Download this eBook to see how an effective CAPA system manages the entire process of evaluation and remediation of serious and possibly systematic quality events.