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Managing your TMF is complicated. Simplify it with a next-generation eTMF system.

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eFeasibility and eTMF platform

Streamline TMF Compliance with the eTMF for Growing Biotech and Pharma Companies

Our AI-powered electronic trial master file empowers every stakeholder - from study managers and CRAs to IT teams and business leadership - to be more compliant. By streamlining TMF compliance, TI eTMF removes the friction from day-to-day clinical operations. Learn how you can ensure quality, completeness, and timeliness with an electronic trial master file.

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Simplify TMF Management & Achieve Inspection Readiness

Streamline compliance with automation

Automate metadata and indexing workflows with machine learning to make inspection readiness easier than ever with 98% accuracy.

Set up your eTMF in a matter of weeks

Launch faster with painless implementation of an eTMF system that takes weeks, not months and 24/7 support.

Improve TMF efficiency and collaboration

Streamline TMF document processing and quality control in a single source of truth for your inspection readiness and decentralized collaboration.

Manage your eTMF anytime, anywhere

Developed by clinical professionals for clinical professionals, our mobile application allows CRAs to perform critical TMF tasks and oversight on the go.

Achieve inspection readiness

Maintain TMF completeness and health with real-time document processes and audit trails.

Reduce timelines and increase transparency

Speed timelines and maintain TMF health with proactive oversight enabled by dashboards, analytics, and mobile insights.

TI eTMF Seamlessly Connects to our 21 CFR Part 11 Compliant eClinical Platform

With built-in content management, site feasibility, study start-up, learning management, and CTMS solutions, you have a complete, central solution for on-site and remote clinical trial management.

eTMF Features.

Reduce the risk of inspection findings with features that simplify trial master file management.

Get the support of on-demand TMF experts and document specialists. Request a Demo >

Leverage ML and AI for document processing, auto-coding, and metadata extraction. Request a Demo >

View planned and actual milestones and tasks in real-time by date, priority, and risk. Request a Demo >

Quickly and securely capture, index, and publish documents to the eTMF, directly from phone or tablet devices.   Request a Demo >

Review real-time TMF insights and oversight to make faster risk-based decisions. Request a Demo >

Enable real-time document processes, version control, and 21 CFR Part 11 eSignatures. Request a Demo >

Simplify onboarding and daily use by managing just one login for all applications and modules. Request a Demo >

Stay on top of the document workstreams and maintain a complete and quality TMF. Request a Demo >

Streamline communication with an Email and Correspondence Inbox. Request a Demo >

Configure your eTMF to custom structure requirements and keep it aligned with the most current standards. Request a Demo >

All features include: QC1/QC2 Step Workflow, Quality Review Audits, Document Query and Task Management, ML Auto-Coding and Extraction, Duplicate Checks and Comparisons, Document Certification and Redaction, Flexible and compliant Metadata configuration, Required Documents and Placeholders, Country, Site, Contact Requirements, Event Manager & Health Tracking, Completeness Views, Study Start Up integration, Email and Correspondence Inbox, Bulk Upload & Migration, Responsible Party, MyTI Mobile App, CRA Reconciliation, Site and Study Collaborate / Content Authoring Request a Demo >

See These Features and More in a Live Demo

eTMF Connections

Experience seamless data flow between eTMF and your systems for Investigator Database and eFeasibility, Content Management, CTMS, Study Start-Up, and Learning Management.

Automatically collect and store site feasibility responses and other essential documentation in the eTMF. Request a Demo >

Seamlessly transition from Study Start Up to eTMF. Request a Demo >

Publish content directly to the eTMF to activate real-time inspection readiness. Request a Demo >

Site and study training documentation is automatically indexed in the eTMF to show training proof to inspectors. Request a Demo >

TI eTMF connects to our full suite of Site Solutions, including eISF and Site Portal, and our QMS. Request a Demo >

See These Features and More in a Live Demo

Essential Features that Support eTMF Health

Quality

  • Review and Indexing Workflow
  • Quality Review Audits
  • Document Query and Task Management
  • ML Auto-Coding and Extraction
  • Duplicate Checks and Comparisons
  • Document Certification and Redaction

 

Completeness

  • Flexible and compliant Metadata configuration
  • Required Documents and Placeholders
  • Country, Site, Contact Requirements
  • Event Manager & Health Tracking
  • Completeness Views
  • Study Start Up

Timeliness

  • Email and Correspondence Inbox
  • Bulk Upload & Migration
  • Responsible Party
  • MyTI Mobile App
  • CRA Reconciliation
  • Site and Study Collaborate / Content Authoring

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

Clinical Trial Assistant, Sponsor

“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

“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

From site identification to close-out, clinical document processes and operational oversight are complex. Our electronic trial solutions simplify your clinical operations: expedite timelines, enable collaboration, improve quality, capture the full story of study, and pass inspections.

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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Latest from our leadership

Webinar

OpTImize ClinOps: The Power of eTMF & CTMS Integration

Disconnected systems create blind spots in trial management that can lead to regulatory inspections or costly delays. AI can now minimize these risks by serving as the connective tissue between documentation and execution.  

Checklist

Essential Checklist for eTMF Archiving

Disconnected systems create blind spots in trial management that can lead to regulatory inspections or costly delays. AI can now minimize these risks by serving as the connective tissue between documentation and execution.  

Strengthening the Backbone of Clinical Trials: The TMF in a Digital World

I’ve just returned from the US CDISC + TMF Interchange in Nashville, where the energy and optimism for the future was undeniable.

Experience Award-Winning Technology

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