About E-Feasibility

TransPerfect customers have successfully leveraged Trial Interactive in hundreds of clinical trials to store critical trial documents as part of the Electronic Trial Master File (eTMF). Trial Interactive is a web-based, mobile-enabled Software-as-a-Service (SaaS) platform offering a suite of eClinical solutions, including eTMF, Electronic Feasibility (E-Feasibility), Content Management, Learning Management, Study Start-Up, Clinical Trial Management, and various other tools essential for clinical trial execution.

The Trial Interactive Platform has the following features:

  • Regulatory-Compliant eTMF Archive: A secure, electronic Trial Master File that meets all regulatory, security, access, and storage requirements across all countries and regions.
  • Fully Hosted & Compliant Solution: Adheres to 21 CFR Part 11, Annex 11, ERES, GDPR, HIPAA, and GxP regulations.
  • Centralized Access to Trial Documentation: Provides a single access point for sponsors and site personnel to manage trial content and documentation.
  • Comprehensive TMF Workflows: Supports key workflows, including document import and coding, quality review, audit and inspection, document certification, and other clinical trial documentation processes.
  • User-Friendly Interface: A thin-client, consumer-grade UI compatible with major browsers, alongside a mobile app supporting both iOS and Android devices.
  • Flexible Document Management: A configurable document management system for Clinical, Quality, and Regulatory documentation, supporting various review and authoring workflows.
  • Integrated Site Identification & Study Start-Up: A suite of tools designed to streamline site identification, feasibility assessment, and study initiation.
  • Comprehensive eLearning System: A full-featured eLearning platform designed specifically for GxP compliance training.

The E-Feasibility module within Trial Interactive facilitates the creation, maintenance, retrieval, and distribution of feasibility questionnaire records for clinical studies. It enables Sponsors and CROs to evaluate the feasibility of conducting a clinical trial in a specific geographical region or site.

Trial Interactive provides a comprehensive, regulatory-compliant, and user-friendly solution to support clinical trials at every stage, from feasibility assessment to study completion.

E-Feasibility provides end-to-end solutions to clinical managers through integration with the Trial Interactive eTMF module.