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Accelerate critical approval, verification, and compliance management processes while ensuring FDA compliance with Tricentis Vera, a leading solution to enhance Digital Validation. 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.
Improve visibility and traceability across testing and CSV activities with Tricentis Vera 2024.2.
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
global life sciences companies
subscription renewals
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.
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.
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.
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.
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.
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.
Enhance CSV by effectively supporting test automation with both pre and post-executional review and approvals of Tosca tests in qTest using Tricentis Vera.
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
