Clin Street eTMF
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eTMF
Streamline clinical trial document management with our secure, compliant eTMF solution.
Ready on Day-1
Pre-configured
Our eTMF solution comes equipped with pre-configured, industry-standard templates and workflows, allowing you to hit the ground running. Say goodbye to expensive setups and lengthy configurations - start managing your documents effortlessly from Day-1.
Seamless Compliance
Effortlessly achieve regulatory compliance with our eTMF solution. With built-in quality workflows, expected document tracking, and real-time KPIs, it ensures your documents are systematically organized and securely managed.
Always Audit-Ready
Stay prepared with easy accessibility, real-time tracking of completeness, quality, and timeliness, dynamic reports, and audit dashboard. Enable sites to directly upload documents and ensure seamless readiness for every inspection.
eTMF Demo
Plan and Manage
- View required documents by study and site milestones
- Easily assign document responsibilities to team members
- Stay informed on document needs based on trial events
- Track document status to ensure timely completion
- Document Analytics to keep document timelines on track
Ready on Day-1
- Minimal training
- Easy to use
- Streamlined workflows
- Effortless document management
- Mobile friendly. Any device
Analytics and Reporting
- Access up-to-date reports for instant trial insights
- Easily visualize essential metrics to drive informed decisions
- Know your document completion status at a glance
- Create tailored dashboards to highlight critical trial metrics
- Document Analytics to keep document timelines on track
Direct Site Upload
- Sites can upload documents directly
- Dedicated dashboard to track documents for every site
- Eliminate misclassified documents
- Timely uploads with automatic reminders and notifications
- Simplify document collection for improved site operations
Streamlined eTMF Archival
- Simplify study closure
- Ensure a seamless transition to the archival phase
- Archive essential documents in just days
- Track all documents end-to-end for full visibility
- Maintain comprehensive and compliant record-keeping
Security by Design
21 CFR Part 11 Complaint
Role Based Access Control
Audit Trail and Version History
Support for Unblinded Documents
Book a Demo
Book a personalized demo to explore the full range of solutions tailored to your needs.
Discover How Our Platform Can Simplify Your Clinical Trials