Computer systems validation (CSV) has been the gold standard for FDA compliance since it was published nearly 30 years ago. However, the tedious, documentation-heavy practices it prescribes impede the adoption of Agile practices. With Tricentis Vera™, life sciences organizations can accelerate their shift to the FDA’s updated computer software assurance (CSA) guidance, supporting Agile testing, reducing excessive documentation, and implementing a risk-based approach to test automation through seamless integrations with Tricentis qTest and Tosca.

In this webinar, we will show you how Vera, qTest, and Tosca can help advance life sciences organizations’ testing and validation maturity to effectively support your shift to streamlined test automation and digital validation – providing a robust software testing and compliance solution.

You will learn how to:

• Overcome roadblocks to adopting Agile practices in computer systems validation
• Drive increased automation coverage for validated apps with pre- and post-execution approvals
• Integrate digital validation into your existing testing workflows with Tricentis Vera, qTest, and Tosca