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Platform Overview

A Faster Way to Launch and Manage Your Clinical Trials

Spending too much time navigating the complexity of clinical trials? Let’s fix that. With a seamlessly connected eClinical platform and complementary support solutions, we enable clinical trial efficiency from site identification to study closeout.
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  • Site Collaboration
  • Remote Monitoring
  • eLearning
  • eISF
  • Site Training LMS
  • Investigator Meetings

Scale Your Clinical Operations with Industry-Leading Technology and Services

Control clinical trial complexity with TI’s eClinical technology and expert services. Our solutions are designed to scale and grow with biotech and pharma companies. With products for every stage of your studies, our seamlessly connected platform simplifies and automates clinical processes for sponsors, CROs, and sites around the world.

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Seamlessly Connected Clinical Trial Software Solutions

Our technologies simplify your clinical operations: expedite timelines, enable collaboration, improve quality, capture the full story of the study and help you 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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The Features You Need for Productivity and Compliance

Consistently Preferred by Clinical Professionals

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

 

Experience Award-Winning Technology

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“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

Latest from our leadership

Checklist

Essential Checklist for eTMF Archiving

Streamline your eTMF archiving process with our comprehensive Archiving Checklist. This essential resource integrates industry best practices and regulatory requirements to guide you through every step, from planning and preparation to post-archival maintenance.

Quick Guide

Preparing for a Regulatory Inspection

This document provides a comprehensive overview of how to prepare for regulatory inspections conducted by agencies such as the EMA, MHRA, and FDA.

Webinar

Trust the Process - TMF Culture

In Season 2, Episode 3 of Trust the Process, hosts Gillian Gittens and Avani Amin welcome Laurel-Ann Schrader, Director of Client Solutions at TransPerfect. Together, they explore how fostering collaboration, ownership, and trust across teams goes beyond just processes.