What's New

TI 10
is here

10+ Years of E-Clinical Innovation.
Millions of documents processed.
Thousands of active eTMFs.
One "author-to-archive platform" for your clinical documents.

Schedule a demo now!

Trial Interactive

Trial Interactive is leading study teams into the future of clinical document collaboration and inspection readiness.

TI10 is powered by a new look and feel that emphasizes transparency, immediate user-defined reporting, and the fewest clicks to action. An author-to-archive approach to document processes captures the complete end-to-end lifecycle from the creation of a document all the way through its ultimate indexing in the eTMF.

There is so much to talk about, but you should really see it for yourself.

TI10 Practical, Powerful Highlights

Simpler. Faster. Smarter.

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eTMF | Clinical Document Collaboration | Quality Documents | Study Start-Up | Document Management | eISF | Compliance E-Learning & Training Management

New Look

New Look and Feel

E-clinical technology that is user friendly. TI10 simplifies the experience without reinventing the wheel for long-time users. Fully responsive and standardized, TI10 works on all major browsers and screen sizes.

On-Demand metrics

On-Demand Metrics

Key data at your fingertips! TI10 displays a set of fully configurable metrics on the home page and room dashboards and allows quick actions to easily address day-to-day tasks. KPI dashboards are available that provide a constant view of eTMF completeness, quality, performance, and health.

Document Collaboration

Author-to-Archive Document Collaboration

A comprehensive approach to inspection readiness. The ability to manage the end-to-end lifecycle of clinical content is a TMF best practice for completeness and inspection readiness. TI10 includes an integrated collaborative authoring interface with "live" editing, review and approval comment features, and ad hoc review workflows.

Document Management

Built-in Document Management

Centralize document processes for improved quality and risk reduction. Configurable room designs deliver fully integrated document management solutions for quality documentation, training management, clinical collaboration, and more. version control, check-in, and the ability to template and publish content between rooms and to the TMF.


E-Learning Interoperability

Create a culture of inspection readiness! For SOP review and approval cycles, the TI GlobalLearn compliance LMS allows you to map courses to content in a content collaboration room and share training groups and certificates with other users. Use GlobalLearn for quality training management, SOP and policy read and understands, study and project training, and patient training.

Content Connector

TI Content Connector

Get connected! A new integration toolset, the TI Content Connector is now supported for interoperability between Trial Interactive and other content management solutions. Flexible metadata translation, publish on binding, and more features make for a seamless integrated solution.

See it yourself.
Schedule a demo.

TI10's Powerful Innovation

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Practical Innovations
of Technology


Automatically classifies documents using machine learning and statistical methods, providing the most likely match and learning from that selection to bulk classify the TMF.

Working View

Shows all draft, in progress, and final documents with missing documents and completeness triggers at a glance to help you stay proactive in managing eTMF health.

Mobile CRA Reconciliation

The mobile myTI app and web-based CRA view simplify the reconciliation process for the CRA on-the-go.

Staging Area

Provides drag and drop of documents to folders and placeholders for easy assignment and classification.

Reportable Views

Flexible views with column selection, advanced filters, saving and sharing, and export capabilities. Configure your own custom reports based on your study specific needs for every grid view in TI.

Document Versioning with Comparison

Improve collaboration with the ability to version and compare documents.

Bulk Coding

Bulk document import and "code as you go," providing a simpler way to upload documents for QC.

These are just a few of our favorite things.
There's so much more!

See it yourself.
Schedule a demo.

Cloud Based | Secure | 21 CFR Part 11 Compliant

Your end-to-end service provider for running streamlined and efficient clinical trials

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