Product Overview
Trial Interactive’s eISF solution reduces administration and improves speed and compliance for site personnel, CRAs, and study teams. Digital investigator site binder processes maintain certified copies of source file documentation and essential documents required for each clinical study. A seamless, connected eTMF allows for automatic indexing of essential documents to the TMF. The ability to conduct remote site monitoring, recommended by the FDA and EMA, helps CRAs work more efficiently in today’s increasingly virtual environment while reducing travel expenses.
Reduce regulatory compliance risks by organizing documents following study-specific requirements.
- Configurable document types, index
- Dashboards & workflows
- Study links to other central vendor & sponsor portals as needed
- Separate, configurable folders for content containing PHI
- Document upload, auto-classification, auto-naming & download
- Location for common reference documents such as protocol, amendments, training materials & manuals
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
- User-friendly dashboard
- 24/7 help desk (email/phone support)
- Start-up (1572, financial disclosure) document Signature workflow
- Learning management system interoperability for site personnel & patient training
- Connected eISF & eTMF rooms
- 21 CFR Part 11 compliant eSignature
- Document de-identification & redaction to protect PHI
- Multiple site access from a single room with controlled, site-specific document access
- Study FAQs to centralize site questions
- Configurable, site-specific reporting
About the company
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.
