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.

eTMF and TMF Services Trial Management Content Management Learning Management

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.

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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.

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News and Press Releases

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

Accelerating Pharma Labeling with Intelligent, Compliant Content

White Paper

Juggling multilingual labels across varying regions and products? Managing the updates and complying with local health authorities' requirements can be a challenge for global pharmaceutical companies, who are facing increasing pressure to streamline labelling processes and digitize labels. This white paper details how a unified eLabeling solution can eliminate duplication, improve accuracy, and deliver measurable ROI. ...

Accelerating Pharma Labeling with Intelligent, Compliant Content
Blog

Health Canada's Transition to XML: What Regulatory Teams Need to Know

In a continued push toward modernization and transparency, Health Canada has entered the next phase of its digital transformation with a mandate requiring the use of advanced extensible markup language product monograph (XML PM) files. This change builds on earlier...
Webinar

LifeSci Talks COA Series | Balancing Innovation and Integrity: AI’s Place in Patient-Focused Research

Artificial intelligence is redefining what’s possible across the clinical development lifecycle, but with rapid innovation comes the need for thoughtful oversight. In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, sits down with ...
White Paper

Web Localization Playbook for Life Sciences

The life sciences industry relies on websites to connect with patients, sites, and global audiences. Whether you're launching a patient recruitment campaign or managing an international healthcare marketing initiative, localization ensures your message is not just understood ...
Webinar

Rewriting the Rules of Informed Consent Development with AI

Regardless of the market a clinical trial is being conducted in, getting locally approved informed consent forms (ICFs) consume as much as 12% of a clinical trial budget before it even begins. Each ICF must be clear and delicately balance local regulations and patient ...
Event

OpTImize London

- | Park Plaza London Westminster Bridge 200 Westminster Bridge Road London, England, United Kingdom, SE17UT ...
Webinar

LifeSci Talks COA Series | Making the Most of Smaller Population Samples: Qualitative Insights in Rare Disease

In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, sits down with Dr. Kate Williams, Director of Patient-Centred Outcomes Research at Acaster Lloyd, to explore the nuances of gathering and applying qualitative data in rare disease ...

Ready to Accelerate Timelines, Improve Quality, and Control Costs?

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