Audit-Ready, Automated Testing for Box

Automate validation and stay audit-ready with ProcessX and Box for life sciences compliance.

• ENTERPRISE-GRADE E-SIGNATURES WITH COMPLIANCE AND AUTOMATION BUILT IN

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).

• ACCELERATE VALIDATION AND ENHANCE QUALITY WITH AUTOMATED WORKFLOWS IN PROCESSX AND BOX

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

• ACCELERATE COMPLIANCE AND STREAMLINE VALIDATION WITH PROCESSX AND BOX

Automated Testing and Validation Workflows

Unify automated testing, Validation Lifecycle Management (VLM), and Application Lifecycle Management (ALM) in a single platform. ProcessX, integrated with Box, empowers organizations to meet global regulatory requirements, reduce manual effort, eliminate process deviations, and ensure audit readiness with real-time dashboards and out-of-the-box compliance reporting.

• AUTOMATED VALIDATION PROTOCOLS AND REAL-TIME REPORTING TO SUPPORT GLOBAL REGULATORY READINESS

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)

Why Automation Scales (or Stalls)

This clip, from USDM’s 2026 Summit, explores how scalable automation starts with strong metadata foundations. Without structured, metadata-driven processes in place, organizations can’t effectively scale automation—at least not without adding significant human effort.

To reach the next level of intelligent, enterprise-wide automation, getting metadata right from the start is essential.

Watch the Summit On-Demand