Discover Our Mobile-First CTMS
Trial Interactive

The Trial Interactive Platform

Trial Interactive provides a practical, author-to-archive approach for streamlining clinical operations, reducing risk, and expediting time-to-market. Clinical professionals around the world consistently choose Trial Interactive as their preferred document management and oversight platform.

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From site identification to close-out, clinical document processes and operational oversight are complex. Our electronic trial solutions simplify your clinical operations: expedite timelines, enable collaboration, improve quality, capture the full story of study, and pass inspections.

eTMF and TMF Services

Speed, scalability, peace of mind: Get industry-leading technology and/or services and stay inspection-ready.

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Content Management

Centralize your document collaboration and management from creation to archival in the eTMF.

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Trial Management

Speed site activation and improve oversight with remote site monitoring and mobile-first CTMS.

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Learning Management

Reduce risk with remote site and study personnel training. Automatically index training records in the eTMF.

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Simpler. Faster. Smarter.

10+ years of eClinical solutions innovation. Millions of documents processed. Thousands of active eTMFs. One "author-to-archive platform" for your clinical documents.

The Power of a Platform

  • Audit Module for Sponsor Oversight

  • Mobile CRA Reconciliation, eTMF Document Capture and Processing, and Content Collaboration

  • Document Auto-Naming and Auto-Routing

  • Predictive Insights

  • Configurable KPIs

  • Configurable Dashboards and Reporting

  • Powerful Document Search

  • Trial Correspondence/Email Capture

  • Query Management

Worried about content and data spread across different systems?

Ask about Our Content Connector
Discover How TI Can Help You Save

Auto-Classification

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

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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.

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Mobile CRA Reconciliation

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

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Staging Area

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

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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.

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Document Versioning with Comparison

Improve collaboration with the ability to version and compare documents.

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Highlights

  • Flexible and Configurable to Requirements

  • Expedites Site Activation and Document Work Streams

  • Comprehensive, Easy-to-Use Workflows

  • Mobile eTMF, CRA Reconciliation, and Document Collaboration

  • Fast Implementation and User Onboarding/Adoption

  • 21 CFR Part 11, Annex 11, ERES, GxP/GCP, GAMP 5, and GDPR Compliant

“We looked at many eTMF systems, but felt Trial Interactive was the most robust for Karyopharm’s global use. It provides real-time access for our global teams and transparency into the status of the TMF for all of our studies. Plus, we have access to Trial Interactive’s other integrated modules as we evolve our process. ”

Sr. Director, Clinical Operations, Karyopharm

Tracey Marshall

We Love Trial Interactive's functionality and workflow in a web-based platform with the ability to meet regulatory requirements to maintain PSMFs for all of our products.

Sr. Director, Global Pharmacovigilance, Aptalis

Catherine Godefroy

Go Remote with Trial Interactive - eClinical cloud solutions across the entire clinical lifecycle.

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Latest from our leadership

Webinar

C3 Study Sessions: Trial Interactive CTMS Demo Webinar

Do you want to improve process and data transparency and reduce cycle times?

Quick Guide

TMF Services Buyers Guide

Ensuring the integrity of your TMF is critical, and placing that responsibility into the hands of a third party is no small decision.

Webinar

C3 Study Sessions: The CTMS Gap - How Systems Forget About Study Managers and CRAs (and How to Fix It)

Study managers and CRAs work in the CTMS daily, are often power users, and hold responsibility for overall study management. Ensuring their success protects budgets, timelines, and mitigates risks. We can make things easier for them!