In pharmaceutical manufacturing, effective CAPA systems are critical for ensuring product quality, regulatory compliance, and continuous improvement. Yet, human errors, fragmented processes, and reactive approaches often limit CAPA’s true potential. This session explores how pharma organizations can strengthen CAPA effectiveness through user-centered workflows, data-driven insights, and AI-enhanced decision support. By integrating AI into CAPA processes, teams can prevent errors before they occur, accelerate root cause analysis, and transform CAPA from a compliance requirement into a driver of operational excellence. In this session, you will learn how to:

• Minimize human errors through streamlined, user-focused CAPA processes.
• Leverage AI to enhance CAPA effectiveness, from root cause analysis to preventive actions.
• Transform CAPA into a strategic quality tool, driving compliance, continuous improvement, and operational excellence.