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Company description

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.

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Software attributed to Trial Interactive

• eTMFView
• CTMSView
• eISFView
• Investigator DatabaseView
• eFeasibilityView
• Study Start-UpView
• myTIView
• eArchiveView
• GlobalLearnView
• Remote MonitoringView
• Site CollaborationView
• Study Records CollaborationView
• Virtual Investigator MeetingsView
• QMSView
• Safety Letter NotificationsView

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