Ace continuous improvement
Prevent recurrence of non-conformance of system and process failures with corrective and preventive actions
CAPA systematically investigates discrepancies – failures and/or deviations – in an attempt to prevent their recurrence. Our CAPA application has been designed to digitize and streamline this process. Our application is in line with FDA requirements and emphasizes Root Cause Analysis, Investigations, and an Action Plan to correct the non-conformance.
Ensure quality with a robustCAPA process
Simplify, streamline, and automate CAPA management
Initiate, assign, review, approve, execute, verify, track, and document the CAPA workflow
Address the issues at hand quickly, comprehensively, and effectively
Reduces reliance on manual tracking and monitoring with an electronic system
Enable faster decision making and actions
Enhance data visibility and daily reminders even outside the app
Increase adoption with easy workflows, fewer screens, color codes, and email notifications
Work with a regulatory-compliant application
Comply with storage requirements of electronic CAPA records and maintain data integrity
Testimonial
The Audree Infotech
Advantage
21 CFR part 11, GAMP 5, and other regulatory compliant
On-going support and user training
Host application on cloud, on-premise, or in a hybrid model
End-to-end validation before go-live
Highly customizable apps as per client processes
Complete suite of pharma apps
Expert-led process consulting
Seamless integration
Faster change request management
Other Applications
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