Go Paperless: Streamline Validation
Digitize your validation processes to enhance efficiency, ensure regulatory compliance, and reduce operational costs. Designed for biotech, pharma, and CRO leaders in IT and regulatory compliance.
Why ProcessX
With more than 25 years of unmatched life sciences expertise, USDM simplifies compliance to drive radical operational efficiency.
ProcessX offers a fully digital, paperless validation solution that eliminates manual errors, accelerates project timelines, and ensures regulatory compliance. Built specifically for biotech, pharma, and CRO organizations, USDM’s solution helps streamline your operations without compromising on GxP standards.
- Fully Digital, Paperless Validation
- Eliminate Manual Errors
- Streamline without compromising GxP
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Accelerate Compliance with a Paperless Validation Platform
Our paperless validation solution is engineered for life sciences leaders looking to improve efficiency while meeting global regulatory standards.
Automated Validation Workflows
Replace paper-based processes with automated workflows that ensure consistency and minimize manual errors.
Real-Time Compliance Monitoring
Stay audit-ready with continuous monitoring and alerts for regulatory compliance risks, ensuring seamless FDA and GxP alignment.
Streamlined Regulatory Documentation
Simplify documentation for audits and inspections with centralized, digital record-keeping accessible across teams and locations.
Cloud-Based Accessibility
Secure, cloud-based platform for easy access to validation documents, enhancing collaboration between IT and regulatory compliance departments.
Faster Time-to-Market
Reduce validation cycle times and accelerate product launches with efficient, fully digital validation processes.
Success Stories
Out-of-the-box Workflows
Choose from dozens of audit-ready, GxP workflows
Single Source of Truth
Manage all GxP, SOX, and non-GxP systems using one a platform