Corrective and Preventive Action (CAPA) is a critical process in regulated industries to identify, investigate, and resolve quality issues while preventing recurrence. Qualityze CAPA Software provides a digital, automated platform to manage the complete CAPA lifecycle efficiently, ensuring compliance, traceability, and continuous improvement.
What is CAPA Software?
CAPA Software helps organizations identify quality problems, analyze root causes, implement corrective actions, and track preventive measures. With Qualityze CAPA Software, companies can:
Capture quality issues digitally
Assign responsibilities and track actions
Perform risk assessments and root cause analysis
Maintain audit-ready documentation
Integrate CAPA with other QMS processes
This ensures that quality issues are resolved systematically and compliance is maintained.
Key Features of Qualityze CAPA Software
Digital CAPA Initiation – Log nonconformances, customer complaints, audit findings, and other quality events.
Root Cause Analysis Tools – Use 5 Whys, Fishbone Diagram, and other methods for problem-solving.
Automated Workflows – Assign tasks, route approvals, and send notifications automatically.
Risk-Based CAPA – Prioritize actions based on severity, occurrence, and impact.
Audit-Ready Documentation – Ensure compliance with FDA, ISO, and 21 CFR Part 11.
Integration with QMS Modules – Link CAPA with Nonconformance, Change Control, Training, and Document Control.
Benefits of Using Qualityze CAPA Software
Improve efficiency in handling quality issues
Reduce operational risks and prevent recurrence
Ensure regulatory compliance and audit readiness
Enable data-driven decision-making
Enhance visibility into quality metrics and trends
Read more - https://www.qualityze.com/capa-management