If you’ve ever been through an audit in the life sciences industry, you know how important Corrective and Preventive Actions (CAPAs) are. Regulatory bodies expect you to have a strong CAPA process in place to uphold product quality and patient safety. But let’s be honest, CAPA management can be one of the most frustrating and time-consuming parts of managing a quality system. I’ve seen companies struggle with manual CAPA processes, disconnected spreadsheets, and never-ending email chains. One...