Intelligent validation for regulated testing
In today’s highly regulated industries, ensuring compliance, traceability, and audit readiness is more important than ever. Companies must demonstrate that their software systems—especially SAP and cloud applications—meet strict validation requirements.
That’s where Tricentis VERA comes in: the digital validation solution that brings automation, transparency, and control to your testing and approval processes.
With Tricentis VERA, you can manage approvals, electronic signatures, and documentation on a central platform—while ensuring full compliance with GxP, FDA 21 CFR Part 11, EU Annex 11, and other global standards.
VERA is an intelligent compliance layer that integrates seamlessly with your existing test management tools such as Tricentis Tosca, qTest, or Jira.
It ensures that every change, every test, and every release in your software lifecycle is properly reviewed, approved, and signed off on—without slowing down your supply chain.
Whether you work in life sciences, pharmaceuticals, medical devices, or any other regulated sector, VERA helps you balance speed and compliance.
V.E.R.A
• Validation
• Execution
• Review
• Approval
Why Tricentis VERA?
Uncompromising compliance
VERA ensures that all validation activities comply with regulatory standards—without disrupting your agile or DevOps workflows.
Consistent transparency
Get real-time insight into the validation progress, approval status, and audit readiness of all projects.
Risk mitigation
Reduce human error, prevent missed approvals, and ensure that every change is reviewed before release.
Seamless integration
VERA integrates seamlessly into your existing ecosystem—from qTest and Tosca to Jira—with minimal setup effort and maximum control.
Efficiency and scalability
Automate manual validation steps, shorten approval cycles, and enable your teams to focus on innovation rather than documentation.
With Tricentis VERA, you can: Accelerate digital validation with full compliance Reduce manual work and shorten validation cycles by up to 70% Ensure full traceability from requirements to results Enable paperless validation for global teams Streamline audits with automated documentation Integrate compliance into DevOps and test automation
Typical use cases
- GxP-compliant validation of SAP or cloud applications
- Automated documentation for audits and regulatory reviews
- Management of electronic signatures for globally distributed teams
- Risk-based validation for faster approvals in regulated environments
Key features
Digital validation and electronic signatures
Replace manual paper documents with secure, compliant electronic signatures that meet FDA 21 CFR Part 11 and EU Annex 11 standards.
Automated review and approval workflows
Define validation workflows that automatically forward test cases, executions, or changes for review and approval—saving time and reducing risk.
Full traceability
Ensure complete traceability across requirements, tests, and results—so every action is ready for audits.
Audit trail and reporting
Every approval, signature, and change is automatically logged. Create audit-proof reports in seconds.
Integration into the Tricentis ecosystem
VERA connects seamlessly with Tosca, qTest, Jira, and other tools, integrating validation and compliance directly into your existing test management environment.
Flexible validation templates
Configure workflows and templates according to your company’s compliance guidelines without having to make complex adjustments.
Conclusion
With Tricentis VERA, compliance becomes a competitive advantage—not a hindrance.
You can rest assured that your systems meet all regulatory requirements while your release cycles remain agile and efficient.
Experience secure digital validation, optimized approval processes, and auditable documentation—all in one intelligent platform.
Take the next step toward modern, paperless compliance.
Optimize your validation process today with Tricentis VERA!
Contact us and get started today!
Konrad Pfadenhauer
Industry Expert & Test Automation Team Lead
If you have any questions about our services for your industry, please contact me for a no-obligation consultation!