Use AI-Powered PERFEQTA to Mitigate Risk Before it Happens
Compliant with FDA, GMP/ GAMP, ISO 9001, and 21 CFR Part 11. Automate the process of reporting, investigating and responding to any deviation from approved procedures. With PERFEQTA you can track deviations from the initiation stage and documentation to review, from investigation to follow-up, and from approval to post-implementation. Group all your documents and related information, and bring the right people together at the right time. Reduce discovery, resolution, and reporting turn-around time and ensure that any deviation from your SOPs is documented for compliance and reduce re-occurrence. Link your deviations to PERFEQTA's QMS apps or other operational apps to get more out of your system.
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