Trial Interactive eClinical Solutions

Choose a faster way to launch and manage your global clinical trials, from site identification to close out.

Expedite Your Study
Doctor using a tablet

Scale your clinical operations with industry-leading technology and services.

Trial Interactive is designed to scale and grow with biotech and pharma companies. With eclinical solutions for every stage of the clinical trial lifecycle, our seamlessly connected platform streamlines and automates essential clinical processes across thousands of studies for sponsors, CROs, and sites around the world.

Speed, scalability, and peace of mind: get industry-leading technology and services to stay inspection-ready. Incorporate a platform that provides flexibility and adaptive trial master file processing.

  • AI Portal
    Industry-leading, AI-powered eTMF
  • Tablet
    Mobile eTMF (myTI)
  • Site Solutions
    Site Solutions
  • TMF 2
    TMF Services
  • Star with a tie
    TMF University
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Expedite site activation and improve oversight with remote site monitoring and mobile-first CTMS.

  • eLearning
    eFeasibility
  • Site Solutions
    Site Solutions
  • Study Start Up
    Study Start-Up
  • Remote Monitoring
    Remote Monitoring
  • CTMS
    CTMS
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Centralize your document collaboration and management across the clinical lifecycle from creation to indexing in the eTMF.

  • Third Party Integration
    Clinical Study Document Collaboration
  • Document Management
    General Document Management
  • Study Team Training
    Quality Documents and Training Management
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Reduce risk with remote site and study personnel training. Automatically index training records in the eTMF.

  • eLearning
    LMS and eLearning
  • Cog Certification
    QMS
  • Study Team Training
    Study Team Trainings
  • Human Resources
    Remote Investigator Meetings
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Controlling Complexity in Clinical Trials

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.

Reducing IT Burden on Small and Mid-Sized Pharma and Biotech

In this webinar, our Head of Product, Jay Smith, discusses the ways in which a complete and connected eClinical platform can help reduce the IT burden for small to mid-sized pharma and biotechs. Topics covered include regulation, compliance, validation, and change management.

News and Press Releases

Our industry experts have in-depth understanding of the challenges, requirements, and goals for life sciences organizations.

Clinical Evidence in Digital Health: Considerations for Multi-Country Evidence Generation

The global adoption of digital health solutions has revolutionized healthcare delivery, offering unprecedented opportunities for innovation in patient care, diagnostics, and disease management. However, the generation of robust clinical evidence to support these technologies across diverse regulatory, cultural, and healthcare system contexts remains a significant challenge. In this webinar, Alexandra Crane, VP of COA, Digital Health, and Regulatory Solutions at ...

Clinical Evidence in Digital Health: Considerations for Multi-Country Evidence Generation

Sanofi’s Journey of Digital Transformation through AI-Powered Translations

The global clinical landscape is becoming more complex every day, with evolving regulations and increased pressure on life sciences organizations to reduce costs and timelines. Join us for an in-depth discussion on how one of the world’s leading pharma companies is leveraging AI ...

Lessons Learned from SCMS Deployments in Global Medical Device Documentation

Transitioning to modular content using a Structured Content Management System (SCMS) has the potential to transform medical device documentation by streamlining authoring and automating content updates and publishing. For a truly successful implementation, however, early planning ...

LifeSci Talks | Measuring What Matters: Modernizing Clinical Outcome Assessments with Patient-Centric Approaches

In this episode of LifeSci Talks, TransPerfect’s Global Practice Leader Mark Wade sits down with Dr. Karl McEvoy, VP of eCOA and Patient Technology at YPrime, to discuss the importance of embracing technology in clinical research to reduce the patient burden. The two cover ...

7 Essential Steps to Reach Global Audiences with Website Localization Services for Life Sciences Organizations

Website Localization for Life Sciences Organizations Means Greater Global ReachLife sciences organizations are under increasing pressure to connect with global audiences. With 65% of internet users preferring websites in their native language and 40% refusing to buy from...

Harnessing AI in Pharmacovigilance: Insights from World Drug Safety Amsterdam 2024

Pharmacovigilance professionals face an escalating challenge: data overload. From AI-powered transcription and case triage to automated literature translation, insights from the World Drug Safety Congress 2024 showcased practical solutions for streamlining workflows and reducing ...

Harnessing AI in Pharmacovigilance: Insights from World Drug Safety Amsterdam 2024

IntroductionIn the pharmacovigilance space, the overwhelming trend in the current landscape is data overload. Increasingly unmanageable volumes of information pose a core challenge for today’s pharmacovigilance professionals. While digital transformation and new technologies...

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