Tricentis Vera
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With Tricentis Vera, organizations can:
Enable 21 CFR Part 11 and FDA compliance
Embed the triggers and controls to capture 21 CFR Part 11 compliant electronic signatures in Agile software testing workflows and accelerate computer systems validation.
Seamlessly synchronize the review and approval process
A centralized UI across tools acts as a single system of record. With Vera, users and teams are able to access a holistic view of their review and approval tasks in real-time.
Increase speed and quality while reducing risk in regulated testing
With technical controls over process and approval flows, regulated organizations are able to drastically reduce their risk of compliance deviation and human error typically associated with manual, document-centric validation.