Manage the Complete Life-Cycle of the Change and Get Insights
Compliant with FDA, GMP/ GAMP, ISO 9001, and 21 CFR Part 11. Automate the process of validation and verification of approved specifications for any product or service you provide. Reduce validation and out of specification investigation turnaround time and share findings with the appropriate members of the team. Assure compliance and completion of investigations and link other management apps in PERFEQTA QMS for a more holistic approach to quality management.
(...Not Weeks, Not Months.)
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