CAPA Management 2021 - Root Cause Analysis Techniques and CAPA Management Training Course

Corrective and Preventative Action (CAPA) is a system of quality procedures required to eliminate the causes of an existing nonconformity and to prevent recurrence of nonconforming product, processes, and other quality problems
Once the RCA identifies the factors that caused the event, proper generation of CAPA actions is critical to maintaining a healthy quality system. The regulatory agencies fully expect to see documented root cause analysis
• Understand Regulatory and Industry Guidance
• What is Root Cause Analysis?
• When Should Root Cause Analysis be performed?
Speaker:
Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations.