CAPA management software can help organizations ensure compliance with relevant regulatory requirements and industry standards. The software can provide automated workflows and audit trails, making it easier to demonstrate compliance and respond to audits. Qualityze CAPA management software is closely tied to quality standards and regulations, such as ISO 9001 and FDA regulations. Compliance with these standards requires effective CAPA management processes that includes incident reporting, root cause analysis, and corrective and preventive action planning.

Qualityze CAPA Management Software eliminates systematic issue like deviations, nonconformances, defects and others by identifying their root causes by successful investigation and makes sure that it won’t occur later. From this Qualityze CAPA Management Software, you can easily perform the following activities like CAPA Initiation, Investigation, Root cause analysis, Risk assessment, Planning & Implement Action Plans, Effectiveness Review, Resolution Activities, Verification, Digital Signature Validation.