CAPA Management System
Corrective and preventive action (CAPA) is the core of any quality system. Effective CAPA management is especially crucial for life science companies and other organizations doing business in regulatory environments. The overall effort to investigate and correct quality issues to prevent recurrence is vital not only to achieving regulatory compliance but also to overall product quality. Maintaining compliance with globally recognized regulatory requirements (such as those set forth by the FDA and ISO) are singularly critical to success. When implemented properly, CAPA management systems can enhance product quality and safety, increase customer satisfaction, and most importantly, ensure compliance with regulatory standards.