With our CAPA software, quality teams get complete visibility into ongoing and closed actions. The system ensures that every task is properly tracked, reviewed, and documented so you're always audit-ready. CAPA not only helps resolve issues but also improves processes to avoid future risks
Why CAPA Matters in Pharmaceuticals
In the pharmaceutical industry, product quality and regulatory compliance cannot be compromised. CAPA ensures that every issue whether a deviation, audit finding, or customer complaint is addressed systematically. Using CAPA software, companies can:
Prevent recurrence with corrective and preventive measures
Ensure all actions are tracked, reviewed, and verified
Stay compliant with global guidelines like 21 CFR Part 11 (USFDA)
Key Features
Manages the complete CAPA lifecycle from initiation to closure.
Web-based access for secure and easy usage across sites.
Electronic Signatures and audit trails as per 21 CFR Part 11 (USFDA).
Standard questionnaires configurable for each department.
Impacted departments can add corrective and preventive actions.
Verification by multiple reviewers; effectiveness check is recorded.
Automated reminders through email and notifications for key dates.
