Learn what CAPA (Corrective and Preventive Action) is and how to use it in quality management. Download free CAPA format, template and examples in Word and Excel. Corrective and Preventive Actions (CAPA) system captures issues, investigates root causes, implements fixes, verifies effectiveness, and logs evidence to satisfy ISO/FDA compliance while driving continuous quality and safety improvements worldwide. Learn what CAPA is, why it's important, and how to implement it step by step. This guide covers the 8-step CAPA process, real-world examples, tools, and tips for avoiding common pitfalls. What Is CAPA (Corrective Action and Preventive Action)? CAPA, which stands for Corrective Action and Preventive Action is a structured process to identify, address, and prevent the recurrence or occurrence of quality and compliance issues. CAPA involves detecting issues such as deviations, nonconformities, audit findings, complaints, or potential issues. CAPA carries out a thorough root cause analysis to understand the underlying problem and implement targeted measures to correct existing ...
