vFile-eTMF™ covers full document life cycle from document creation to document review, approval and validation.
Essential trial documentation is, unquestionably, one of the most critical requirements associated with conducting a clinical trial. It is also time consuming and expensive activity.
Enable active TMF management and oversight for real-time inspection readiness, visibility, and control. vFile-eTMF™ is cloud-based, solution that includes sources defined in the Drug Information Association’s (DIA) eTMF Reference Model.
vFile-eTMF™ covers full document life cycle from document creation to document review, approval and validation, also controls distribution, versioning and eventual archival.