Minimize Your Veeva Compliance Burdens, Maximize Efficiency

Automate validation and stay audit-ready with ProcessX and Veeva 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

Veeva Vault manages content and data in a single platform and enables life sciences organizations to deploy powerful applications that manage processes with related content, data, and workflows. USDM’s industry expertise ensures the program is expertly managed, implemented correctly, and adopted across the organization. ProcessX takes your Veeva Vaults even further.

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

ProcessX and Veeva

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 VEEVA

Automated Testing and Validation Workflows

Unify automated testing, Validation Lifecycle Management (VLM), and Application Lifecycle Management (ALM) in a single platform. ProcessX, integrated with Veeva, 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)

As a Premiere Services Partner of Veeva, USDM can also assist with expert program management, end-user training and communication, data migration, content governance, and post-go-live configuration and change management. For companies distributing medical devices, USDM’s global UDI services and Veeva’s UDI offerings assess your as-is state, provide regulatory and process guidance, and drive the transition to your to-be state.  

Get in touch with our team to optimize your GxP processes today!