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.
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
How we do it
Apply technical controls, 21 CFR Part 11 compliance, and configurable review and approval routes for compliance in your designated GxP software projects.
Automate your software testing without sacrificing compliance through controlled review/approvals of test and execution results.
This tight integration allows Vera to control Jira and qTest data while standardizing approval lifecycles, all without restricting core functionality or requiring customization.