The DRS electronic Trial Master File (eTMF) provides a secure, compliant, and highly configurable platform for managing essential clinical study documentation.
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Supports multiple custom file structures and can be implemented on an accelerated timeline to meet sponsor and CRO needs.
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Ensures documents are captured, organized, and maintained in accordance with ICH‑GCP and global regulatory expectations.
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Includes a built‑in archiving module for long‑term retention and inspection‑ready access.
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Provides real‑time visibility into document status, completeness, and compliance across all study phases.