Capa:

CAPA, or Corrective Action and Preventive Action, is a systematic approach to identify, resolve, and prevent issues. A CAPA form serves as a structured tool to document and implement CAPAs when a recorded issue or nonconformance is detected. 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 ... CAPA is a process which investigates and solves problems, identifies causes, takes corrective action and prevents recurrence of the root causes. Learn more about CAPA. 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.