Traditional document-centric approaches to computer systems validation continue to limit life sciences organizations as they modernize software delivery processes. In this webinar, we will show you how modernizing compliance with Tricentis Vera to support Digital Validation allows teams to shed cumbersome documentation practices by seamlessly embedding compliance management features into leading tools, such as Tricentis qTest and Atlassian Jira.
In this webinar, you will learn:
- How shifting to Digital Validation supports quality, not documents
- How Tricentis Vera helps you meet business objectives while satisfying compliance requirements
- How you can easily implement electronic signatures, automated review and approvals process, and technical controls across the development and testing toolchain