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Tricentis Vera™

Modernizing software compliance in Life Sciences

Accelerate critical approval, verification, and compliance management processes while ensuring FDA compliance with Tricentis Vera, a leading Digital Validation solution. Unlike traditional e-signature and document-centric processes, Vera enhances the software validation process with an approach that is designed for modern Agile and DevOps environments.

We got you covered for Agile validation

Get a limited time offer of the first three months of qTest Enterprise free when purchasing a 12-month subscription of both qTest Enterprise and Vera.

More than just electronic signatures

With Tricentis Vera, Digital Validation means more than just applying electronic signatures to shift traditional documents to a computer screen. It means modernizing the Computer Systems Validation process to shed cumbersome, extraneous documentation practices and enabling compliance to be achieved as a byproduct of good software quality practices.


users around the globe


utilized by nearly all top 20 global life sciences companies


subscription renewals


How we do it

21 CFR Part 11 Compliance

Embed the triggers and controls to capture 21 CFR Part 11 compliant electronic signatures in Agile software testing workflows and accelerate time to market with Tricentis Vera.


Central review and approval portal

With Vera providing a centralized UI across tools and acting as a single system of record, users and teams are able to access a wholistic view of their review and approval tasks in real-time.


Tightly integrated with qTest and Jira

The integration between Tricentis qTest and Jira becomes even more powerful for regulated teams with Tricentis Vera. Now, Agile planning and continuous testing workflows can be used across both regulated and non-regulated systems.


Lock records down

Once validation assets are either routed for approval or approved, the records will be locked in both qTest and Jira to ensure no edits are made to that record during or after the approval process.


Generate auditable electronic records

By capturing and generating system based electronic records containing all associated validation data and audit history, teams can shed their reliance on disruptive, extraneous paper or electronic document-centric processes.


Compliance designed technical controls

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.


Integrate Vera into your Agile and automation tools

Learn more about Tricentis Vera