Audree Infotech Pvt. Ltd.

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

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Insights

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10.02.2021

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10.02.2021

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10.02.2021

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podcast

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10.02.2021

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Get Started On Your Transformation With Audree Infotech