Data Reduction Systems
DRS Corporation has been providing professional services and software solutions to the clinical drug research market for 40 years. They support worldwide clinical trials through their electronic Trial Master File (eTMF) platform, document processing services, study transfers, and archiving solutions. Their mission is to support sponsors and CROs in managing clinical trial documentation efficiently, ensuring regulatory compliance, and maintaining study integrity.
Industries
Nr. of Employees
medium (51-250)
Data Reduction Systems
Products
eTMF software platform
A configurable electronic trial master file system supporting multiple file structures, integration with the TMF Reference Model, streamlined document submission workflows, automated QC notifications, and study activation capabilities.
TMF Archive Viewer module
Hosted module for long-term storage and access of closed studies that preserves folder structure, metadata, and audit records and provides search and read-only access across archived content.
eTMF software platform
A configurable electronic trial master file system supporting multiple file structures, integration with the TMF Reference Model, streamlined document submission workflows, automated QC notifications, and study activation capabilities.
TMF Archive Viewer module
Hosted module for long-term storage and access of closed studies that preserves folder structure, metadata, and audit records and provides search and read-only access across archived content.
Services
Rapid deployment and configuration of an eTMF platform with support for multiple file structures, TMF Reference Model alignment, study activation, and user access management.
Operational processing of TMF documents including attribution, QC review, automated error reporting, and remediation workflows to enforce good document practice.
Consolidation of closed or older studies into a hosted archive with read-only access, search capabilities, and long-term storage from a Tier 3+ data center.
Migration of TMF libraries between systems or into sponsor archives, reconciliation for acquisitions or CRO offloads, and provision of migration documentation to verify integrity.
Scanning of clinical paper binders into electronic formats following ALCOA+ guidelines, including page-by-page comparison certification and upload with metadata application.
End-to-end auditing of eTMF content and risk-based assessments to identify missing documents, metadata attribution issues, and filing inconsistencies to support inspection readiness.
Rapid deployment and configuration of an eTMF platform with support for multiple file structures, TMF Reference Model alignment, study activation, and user access management.
Operational processing of TMF documents including attribution, QC review, automated error reporting, and remediation workflows to enforce good document practice.
Consolidation of closed or older studies into a hosted archive with read-only access, search capabilities, and long-term storage from a Tier 3+ data center.
Migration of TMF libraries between systems or into sponsor archives, reconciliation for acquisitions or CRO offloads, and provision of migration documentation to verify integrity.
Scanning of clinical paper binders into electronic formats following ALCOA+ guidelines, including page-by-page comparison certification and upload with metadata application.
End-to-end auditing of eTMF content and risk-based assessments to identify missing documents, metadata attribution issues, and filing inconsistencies to support inspection readiness.
Expertise Areas
- eTMF implementation and management
- TMF archiving and migration
- Clinical document quality control and validation
- Inspection readiness and regulatory TMF auditing
Key Technologies
- Electronic trial master file systems
- Hosted archive viewer modules (data center hosting)
- Document scanning and digital certification workflows
- Metadata management and indexing