E-Clinical Technologies

GLOBAL eCLINICAL SOLUTIONS

Support your clinical research and trials with TransPerfect Life Sciences’ eClinical Technology, Trial Interactive. Trial Interactive is an industry leader in practical, global eClinical innovation that simplifies and automates clinical processes for sponsors, CROs, and sites around the world. The 21 CFR part 11 compliant unified platform delivers an author-to-archive collaboration experience with solutions for clinical document management, site selection, site activation, e-learning, compliance training, quality, and more with seamless solution interoperability and indexing to the eTMF. Trial Interactive is consistently selected by clinical professionals for providing the most comprehensive yet intuitive experience with the most complete offering of technology and expert TMF services. Trial Interactive helps study teams streamline their operations by cutting unnecessary expenses, expediting timelines, reducing compliance risks, and improving operational excellence.


Your Perfect-Fit, Author-to-Archive Platform to Improve Speed, Compliance, Quality, and Oversight.

eTMF and TMF Services

Speed, scalability, peace of mind: Get industry-leading technology and/or services and stay inspection-ready.

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Content Management

Centralize your document collaboration and management from creation to archival in the eTMF.

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Trial Management

Speed site activation and improve oversight with remote site monitoring and mobile-first CTMS.

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Learning Management

Reduce risk with remote site and study personnel training. Automatically index training records in the eTMF.

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TransPerfect Life Sciences’ industry-leading platform built by clinical professionals, for clinical professionals

  • Flexible and Configurable to Requirements
  • Expedites Site Activation and Document Work Streams
  • Comprehensive, Easy-to-Use Workflows
  • Mobile eTMF, CRA Reconciliation, and Document Collaboration
  • Fast Implementation and User Onboarding/Adoption
  • 21 CFR Part 11, Annex 11, ERES, GxP/GCP, GAMP 5, and GDPR Compliant

Simpler. Faster. Smarter.

10+ years of eClinical solutions innovation. Millions of documents processed. Thousands of active eTMFs. One "author-to-archive platform" for your clinical documents.

  • Content Management/Clinical Document Management
  • eFeasibility
  • Study Start-Up
  • Learning Management (LMS)
  • Remote Investigator Meetings
  • eTMF with Mobile CRA App
  • TMF Services
  • eISF/Site Portal with Mobile CRA App
  • Mobile-First CTMS
Request a Demo Today
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