Microsoft Validation Suite
Enterprise Content Management systems provide a platform for creating, editing and managing critical business documents for an organization. Knowing where documents are, controlling access to them, finding them quickly, linking them to business processes, and archiving or destroying them at the right time in their lifecycle are fundamental requirements for regulated industry.
Our Validation Accelerator Package (VAP) provides validation assistance with core regulatory requirements for the following modules:
- Document Management System
- Quality Management System
- Regulatory Document Module
- Clinical Document Module
- SOP Management Module
USDM's NextDocs ECM VAP documentation provides a pre-configured content rich set of templates, ready for customization to meet both domestic and international regulations. Our documentation templates include:
- Validation Plan
- User Requirements Template
- Risk Assessment
- Functional and Design Specification
- Installation Qualification
- Operational Qualification
- Performance Qualification Template
- Trace Matrix
- Validation Summary Report
USDM works closely with NextDocs to identify upcoming patches and updates, and provides a full maintenance program for our NextDocs ECM clients. Recommendations for required testing are made to ensure our clients an effective, efficient validation maintenance process.
USDM has a dedicated, experienced ECM validation team that can customize the VAP templates and provide best practice consulting on regulatory compliance.
To learn more about USDM and how we can assist with your compliance and business objectives, please contact:Rebecca Meledy
888.231.0816 x161
775.213.5943 (fax)
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"Simplify, Unify and Optimize your business & compliance needs with USDM"
