Discover Our New CTMS
Trial Interactive

eTMF

Set up your eTMF in a matter of weeks!

A practical, secure, and compliant single access point for TMF documentation, supporting all essential document processes and reducing TMF management timelines, costs, and risks. The Trial Interactive eTMF provides study teams of all sizes the author-to-archive experience necessary for quality and completeness. A powerful 21 CFR Part 11 compliant collaboration environment enables not just timely, but real-time, document processing with an inspection-ready data lineage and audit history.

Request a Demo

TMF Experts and Document Specialists On-Demand

Industry Leading Technology with an Award-Winning User Experience

Developed by Clinical Professionals for Clinical Professionals

eTMF Highlights

  • Configurable TMF Reference Model Support
  • Simplified Auto-Coding and Auto-Naming
  • Milestone and Task Management
  • Mobile App with CRA Reconciliation Support
  • TMF Health, KPIs, and Ad Hoc Dashboards
  • CTMS and IRB Integration and Submissions
  • Corporate Directory Integration with Single Sign-On
  • Active Alerts and Notifications
  • Email Correspondence Capture 
  • Supported by Comprehensive TMF Services
  • Compliant with Global Regulations
  • Document Management and Authoring
Learn More

eTMF Features

  • Real-Time Collaboration

  • Fast Implementation

  • Secure and Compliant

  • Low Cost of Ownership

  • Audit and Inspection Readiness

  • Risk Reduction for Inspection Findings

  • Real-Time TMF Insights and Oversight

  • Reduction of Administrative Burdens

“Our search for an eTMF solution required that we find a product that met DIA requirements and was designed and backed by people who truly understand the world of clinical trials. The claims made by the Trial Interactive team during our evaluation process were proven overwhelmingly true; it’s easy to use, provides us with significant insight into TMF completeness, and reporting on key data is simple and comprehensive. Trial Interactive has without question improved ARCA’s ability to complete trials in the most efficient manner possible.”

Eric Negrey, Senior Director of IT and Facilities at ARCA Biopharma

“It's very user-friendly and easy to use the system.”

Clinical Trial Assistant, Sponsor

”That system ROCKS! That was the easiest regulatory I’ve done yet! I hope in the future all trials are done this way.”

Penelope K. Manasco, M.D., CEO, Mana RBM

Practical Innovation: Applying AI and Machine Learning Where It Really Works

Make sure you know what machine learning in the eTMF can really do to streamline your operations.

Make sure you know what machine learning in the eTMF can really do to streamline your operations.

Get in Touch
Learn more about How AI and ML can help you

Case Study

US-Based Biotech with 300 Employees Gains Drug Approval

A Pivotal Phase III Study with 640 sites in 30 countries

Read More
Ask a Question