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.

Trusted by Life Sciences Organizations Big and Small

Join TransPerfect's community of over 1,000 life sciences organizations, including pharma, biotech, CROs, IRBs, and agencies.

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

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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.

Four Years In: What the EU Clinical Trial Regulation Has (and Hasn't) Delivered

When the EU Clinical Trial Regulation (EU CTR No 536/2014) went live for new submissions on January 31, 2022, it promised to transform how clinical trials are authorized and conducted across Europe: a single submission, one decision, and harmonized oversight. Four years in, the reality is more nuanced. The regulatory landscape, meanwhile, is moving faster than ever. In a recent Xtalks webinar, four subject matter experts with direct experience navigating CTR and ...

Four Years In: What the EU Clinical Trial Regulation Has (and Hasn't) Delivered

IMP Labeling Workflows That Reduce Relabeling Risk and Start-Up Delays

Investigational medicinal product (IMP) labeling sits at the heart of clinical trial supply, impacting departments across pharmaceutical organizations, from clinical operations and regulatory affairs to quality assurance and beyond. When labeling activities are managed across ...

The Missing Link: Why Study Design Makes or Breaks a Clinical Trial

In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, sits down with Farrell Healion, Founder and Principal Consultant at OptiTrial, to explore why study design is so often the overlooked "missing link" in clinical ...

C3 Summit 2026 - London

Conversations on Clinical Content, C3 Summit is part of a series of events hosted by TransPerfect Life Sciences featuring sessions with expert panels discussing present challenges, strategies, and innovations, as well as insights into future advancements, from R&D to ...

Considerations for eCOA in Global Clinical Trials

Regulatory Considerations for eCOA Submissions in Global Clinical Trials: What You Need to KnowWhen managing eCOA in clinical trials across multiple countries, translation, linguistic validation, and electronic implementation of Clinical Outcome Assessments (COAs) are...

Xtalks | EU Clinical Trial Regulation: Latest Developments and Upcoming Opportunities

The EU clinical trial landscape has changed significantly since Regulation (EU) No 536/2014 became applicable on January 31, 2022, and sponsors now need a clear view of how the framework is operating in practice and where it may evolve next. This webinar explores the current ...

Veeva RIM TMS Integration Checklist

If your regulatory team is still downloading documents from Veeva Vault, managing translation requests by email, or tracking submissions in spreadsheets, there's a better way. Reduce complexity, close compliance gaps, and shorten your submission cycle times with this ...