Tune in on October 30th, 2025 to stay ahead of the curve with the newest Tricentis Vera™ features designed to simplify compliance, validation, and testing workflows in regulated environments.
In regulated industries, balancing innovation with compliance can be complex. Tricentis Vera™ continues to simplify this challenge by digitizing validation and approval of workflows — reducing manual effort while maintaining full compliance with standards such as FDA 21 CFR Part 11, EU Annex 11, and GxP.
In this Expert Session, you’ll discover the latest Vera enhancements that help teams manage requirements, test, execution, and defect approvals without the need to integrate with Tricentis qTest — ideal for COTS and non-product validation scenarios.
You’ll also learn how to:
- Simplify CSV and CSA processes by using qTest and Vera together for end-to-end approval management.
- Reassign approvals to individual assignees to ensure the right resources review and approve work efficiently.
By the end of this session, participants will be able to:
- Identify the newest Tricentis Vera features and enhancements
- Explain how these updates streamline requirements, test, execution, and defect approval processes
- Describe how Vera simplifies CSV and CSA workflows without requiring full integration
- Understand how to reassign approvals to ensure accurate resource accountability
To get the most out of this session, we recommend attendees have:
- Basic familiarity with Tricentis Vera
- A general understanding of compliance and validation processes in regulated industries
Speakers:
- Henry Farris, Senior Director, Product Management at Tricentis
- Abigail Kurtzman, Product Marketing Manager at Tricentis
