Built leveraging 35 years of Clinical Trial experience
ComplyDocs eTMF helps minimize the risk and complexity of managing large amounts of clinical trial documents. Identify, centralize, review and manage documentation all in one place to ensure it is complete, high-quality, and filed on time.
CORE FEATURES INCLUDE
Secure & Compliant
Role-Based Access
TMF content is maintained in a secure, compliant environment with controlled access, configurable user roles, and a complete audit trail capturing all system activity.
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Review & QC Workflow
Retrieval
Built-in workflow routes documents through a QC review process, reducing manual work and ensuring quality issues are resolved as they arise – not weeks or months later.
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Real-Time Dashboards & Reports
Gain real-time insight into the health of your TMF with simple, easy-to-navigate reports. Identify problems as they occur. Upload and share documents, find out what is completed and what is missing.
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Support for TMF Reference Model
ComplyDocs eTMF has built-in support for the DIA TMF Reference Model; identifying & classifying trial documents, providing a standard set of categories and metadata.
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INDUSTRY RELATIONSHIPS
ComplyDocs eTMF: easily manage clinical trial documents
Easy to Use
Navigation is intuitive and familiar, Fully integrated with Outlook, Role-based dashboards makes it configurable for everyone, Status overviews can be configured easily, Minimal training required
Quick to Implement
Configured based on the TMF reference model, Training Guides and Videos, Quick implementation guides, Product experts on hand, Adjustable based on your requirements.
Affordable to Deploy
Packages that meet anyone’s budget, deployment is not resource heavy, hosting option eliminates additional tech costs, deploys in days/weeks, not months
