Audit-Ready, Automated Testing for Box
Get automated testing, validation lifecycle management, and application lifecycle management in a single app.
Box GxP supports a variety of life sciences use cases, including contract research organization (CRO) and contract manufacturing organization (CMO) collaboration, clinical collaboration, clinical dataset management, Quality document management, mergers and acquisitions (M&As), and post-merger integration (PMI).
ProcessX & Box
By automating testing, Validation Lifecycle Management (VLM), and Application Lifecycle Management (ALM) in ProcessX, you’re able to:
- Integrate VLM and change control to eliminate process deviations
- Access real-time dashboards to see the status of a release and compliance activities
- Achieve faster test execution to free your team of burdensome validation tasks
- Enable workflow-enforced Quality by Design
- Streamline collaboration between IT, quality, and business teams
- Experience fewer data-entry errors by digitalizing and automating paper-based workflows
- Improve quality with regulatory requirements management using AI
Automated Testing & Validation Workflows
Regulatory Artifacts and On-Demand Reporting
ProcessX delivers out-of-the-box reporting templates and dashboards that save you time and give you peace of mind that you are audit-ready at a moment’s notice. Regulatory artifacts and reports include:
- Validation plan
- Requirements (with detailed risk assessment applied)
- Risk-based automation and configuration verification tests (IQ, OQ, and PQ)
- Traceability reports (generated in real-time to maintain full visibility digitally or via extracted matrices)
- Validation and verification protocols for initial validation and subsequent release management (the reports contain all mitigation evidence, risk assessments, traceability, and rationales for the release)
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To improve regulated content management and maximize the return on investment of Box in your life sciences organization, USDM offers comprehensive services and solutions.