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5 tips for using Xray Cloud in Regulated Industries

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Learn 5 strategies for using Jira + Xray in a regulated environment:

Add Jira workflow controls to your Xray entities

Safeguard your test cases and evidence from unauthorized modifications or deletions. Learn how to configure your Xray workflows to prevent users from editing or deleting records locked by signatures.

Integrate electronic signatures

Streamline your test approvals and eliminate bottlenecks in your testing process. Learn how to integrate Xray with an electronic signature tool to approve your test plans, test cases, and test evidence directly in Jira.

Enforce pre-approval of test cases

Comply with industry best practices by enforcing that test cases are reviewed and approved before execution. Learn how to configure Xray’s execution controls to verify that test cases are in the correct status before testers run them.

Create test coverage

Monitor real-time test coverage of your requirements as your release progresses. Learn how to create test coverage directly inside Jira, including roll-up test coverage from lower- to higher-level requirements. Also, see how to use this test coverage to create an industry-standard Requirements Traceability Matrix (RTM) at release time.

Build single-click test reports

Accelerate your release process by automating your test summary reports. Learn how to use Xray’s Document Generator to create industry-standard testing reports, such as a Test Summary Report, a Test Details Report, and a Requirements Traceability Matrix.

Your instructors:

Sofia Neto

Sofia Neto
Director of Customer Success Xray
Sofia is the Director of Customer Success at Xray (since 2021) and a former Atlassian consultant with more than 15 years of experience with Jira and Atlassian Marketplace apps. Sofia helps customers get the most out of Xray while actively gathering and amplifying their feedback to serve as the voice of the customer and drive continuous product improvement.

Aaron Morris
Founder agile-innovations.tech
Aaron is a software engineer with more than 15 years of experience in the life sciences industry. He specializes in helping FDA-regulated software teams modernize their development processes while complying with industry regulations.

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