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.