Trial Interactive
eClinical operations, regulatory compliance, and trial management for clinical trials—from site activation to inspection readiness.
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Overview
Trial Interactive is an award-winning eClinical platform and TMF services provider purpose-built to simplify the complexity of global clinical operations. The platform serves sponsors, CROs, and research organizations of all sizes, helping them manage regulatory compliance, inspection readiness, content management, site collaboration, study team and site training, quality management, and site activation — all within a single, unified system.
From site identification through study close-out, Trial Interactive's electronic trial solutions are designed to expedite timelines, enable cross-functional collaboration, improve quality, capture the full story of a study, and support successful regulatory inspections. The platform is trusted by organizations ranging from large enterprises to emerging biotechs, and is recognized for reducing operational friction and accelerating clinical innovation.
Core Products and Modules
- eTMF and TMF Services: Industry-leading electronic Trial Master File technology combined with expert managed services, delivering speed, scalability, and peace of mind to keep studies inspection-ready at all times.
- Content Management: Centralizes document collaboration and management across the entire document lifecycle, from creation through review and archival into the eTMF, ensuring all records are organized and accessible.
- Trial Management (CTMS): A mobile-first Clinical Trial Management System that accelerates site activation and improves operational oversight through remote site monitoring capabilities.
- Learning Management: Enables remote training for site personnel and study teams, reducing risk through compliance-focused training programs, with training records automatically indexed in the eTMF.
Key Capabilities and Platform Strengths
- All clinical content creation, review, archival, and training can be managed within one integrated system, eliminating the need to touch documents multiple times across disparate tools.
- Seamless document flow between modules — including GlobalLearn, the eISF, and the eTMF — enables near real-time oversight without requiring on-site visits.
- The platform is designed to make it easy to demonstrate the full story of a study to regulatory agencies during inspections.
- Supports remote trial management, providing visibility into all documents needed to oversee a clinical trial from a distance.
- Rapid deployment capabilities, with clients reporting go-live timelines as short as two weeks, enabling time-sensitive research to proceed without delay.
- Supports adverse event management through compliant safety portal integrations, enhancing workflow efficiency for pharmacovigilance processes.
Notable Customers and Testimonials
- MANA RBM: Leverages Trial Interactive to enable remote trial management with seamless document flow and near real-time oversight, lowering risk across studies.
- Orphan Reach: Deployed Trial Interactive in two weeks, coinciding with a 48-hour MHRA approval following final protocol submission, demonstrating the platform's ability to support expedited, time-sensitive research.
- Sentrx: Collaborated with Trial Interactive to build a fully compliant safety portal platform designed to enhance adverse event management workflow efficiency.
- Trusted by senior leaders at CROs who value the platform's deep understanding of clinical operations details.
Thought Leadership and Industry Engagement
- Trial Interactive publishes regular blog content and hosts expert webinar series, including topics such as rethinking TMF strategy in light of the 2024 EMA GCP Inspectors Report and the evolving role of AI in clinical trials.
- The company offers an Ask an Expert TMF Series through TransPerfect Life Sciences, providing live Q&A sessions on topics such as risk-proportionate oversight.
- Trial Interactive's leadership actively addresses how AI can be embedded invisibly into clinical workflows, moving beyond chatbot functionality toward true co-pilot capabilities for clinical operations teams.
Trial Interactive is part of the TransPerfect Life Sciences ecosystem and continues to evolve its eClinical platform to meet the growing demands of global clinical trial management, regulatory compliance, and inspection readiness across the life sciences industry.
Software
CTMS
Real-time study planning, site monitoring, and compliance tracking for clinical trial operations with mobile-first oversight and integrated eTMF connectivity.
eArchive
Secure eTMF archival and long-term clinical trial document storage with automated retention, regulatory compliance, and audit-ready access.
eFeasibility
Configurable study surveys and Clinical Disclosure Agreements with automated site scoring, real-time reporting, and secure document capture for clinical trial feasibility.
eISF
Digital investigator site binder for organizing and managing essential clinical trial documents with remote monitoring, compliance tracking, and seamless eTMF integration.
eTMF
AI-powered Trial Master File management with automated document processing, 98% metadata extraction accuracy, and real-time inspection readiness for clinical trials.
GlobalLearn
Training management and certification for clinical trial teams on protocol, regulatory, and SOP compliance with real-time compliance dashboards.
Investigator Database
Identify and qualify clinical research sites globally from 300,000+ investigators and 100,000+ sites, with search filtering, historical data integration, and feasibility workflow automation.
myTI
Mobile eTMF capture and publishing for clinical trial teams, enabling CRAs to securely document, index, and upload study records directly from site.
QMS
Issue processing, management, and oversight for clinical trials with incident logging, investigations, CAPAs, and audit tracking.
Remote Monitoring
21 CFR Part 11 compliant remote document verification and management for centralized clinical trial monitoring, with secure site portal and mobile submission.
Safety Letter Notifications
Automated distribution, tracking, and acknowledgment of safety letters for clinical trial sites, ensuring regulatory compliance and timely investigator notification.
Site Collaboration
Secure document sharing and real-time collaboration for clinical trial sites, CROs, and sponsors with 21 CFR 11 compliant eSignatures and version control.
Study Records Collaboration
Secure clinical document authoring and approval for trial teams, with seamless integration to TMF, LMS, and study startup systems.
Study Start-Up
Accelerate clinical trial site activation with automated document management, regulatory submission, timeline forecasting, and obstacle identification.
Virtual Investigator Meetings
Remote investigator training and meeting management integrated with learning management for clinical trials, reducing travel costs and improving attendance.