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See how Tricentis Vera helps ensures FDA compliance
Tricentis Vera
In this 5-minute product tour video, you will learn how Tricentis Vera helps you accelerate computer systems validation with an approach that is designed to be a part of Agile and DevOps workflows. With Vera, you can embed triggers and controls to capture compliant electronic signatures through a single system of record that integrates with test management and Agile planning tools.
All episodes
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Shifting left in life sciences: Optimizing computer systems validation for FDA
Dori Gonzalez-Acevedo, Jason Secola
In this webinar, ProcellaRX Co-Founder and CEO Dori Gonzalez-Acevedo will share best practices for effective transformation. She’ll cover what a modern approach to quality engineering and risk assessment should look like, as well as how you can leverage process and technology improvements to enhance CSV and ensure successful adoption. You will also hear from LifeScan’s Ed Hein about how his team implemented digital validation and a modern approach to quality to both deliver faster and improve compliance.
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Digital Validation: Achieving modern FDA compliance for modern testing
Jason Sencola, John Berek
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.
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Implementing effective test automation in CSV environments-ensure FDA compliance
Jason Sencola, HB Farris
Traditional computer systems validation (CSV) is time consuming, expensive and doesn’t lend itself to modern testing and the effective adoption of test automation. However, with Tricentis Vera, life sciences organizations can modernize their approach to CSV to support agile testing and test automation through our recent enhancements in the qTest and Tosca integration.
In this webinar, we will show how Vera and qTest can help advance life sciences organizations’ testing and validation maturity to effectively support test automation with Tosca – providing a robust software testing and compliance solution.
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Bridging the gap between regulatory FDA compliance and modern software delivery
Kevin Thompson, Jason Tepfendardt
Tricentis and Tx3 executives share the details of Tricentis’ just-announced acquisition of Tx3, which extends our industry-leading continuous testing portfolio with automated digital validation for life sciences and healthcare organizations.
In this webinar, you will learn how the two companies are coming together to enable FDA-regulated organizations to modernize application delivery and reduce risk by integrating digital validation and compliance management with Agile and DevOps workflows. Our executives will share what this acquisition means for our customers and the life sciences industry, as well as how you can leverage Tx3 to modernize your software delivery processes, while dramatically reducing the time and expense associated with traditional validation methods.
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See how Tricentis Vera helps ensures FDA compliance
Tricentis Vera
In this 5-minute product tour video, you will learn how Tricentis Vera helps you accelerate computer systems validation with an approach that is designed to be a part of Agile and DevOps workflows. With Vera, you can embed triggers and controls to capture compliant electronic signatures through a single system of record that integrates with test management and Agile planning tools.