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.


ComplyDocs Screenshot


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

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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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


ComplyDocs eTMF is Easy to use – Quick to Implement – Affordable to Deploy.