Flipping the V Model in software testing for life sciences: A modern, compliant approach

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

Speakers:

• Kirby Lewis, Account Executive
• Alfred Querubin, Solution Architect