Florence's eTMF: Streamline Trial Master File Documentation And Integrate With Sites
Streamline your Trial Master File (TMF) documentation, integrate with study sites to boost quality and accelerate start-up across all your studies.
Adoption
They claim ease of use…but you need a solution that’s straightforward to implement and trains your team quickly.
Flexibility
They claim standardized workflows…but you need a system that adapts to your unique processes without forcing conformity.
Collaboration
They claim site connectivity…but you need a platform sites actively engage with and CRAs can monitor efficiently.
Discover how Florence’s eTMF boosts quality and accelerates start-up across all of your studies.
See how it works
Simplify and accelerate study start-up
Quickly configure your eTMF with intuitive workflows, flexible access controls, and powerful document tools.
- Align templates and naming with TMF structure
- Set permissions for internal and external teams
- Create, edit, sign, and review documents in one platform
Enhance TMF completeness and quality
Gain complete visibility into TMF status and study progress with advanced dashboards and document views.
- Instantly view missing or expired TMF documents
- Sync documents directly into the eTMF via email
- Leverage Part 11 compliant eSignatures
Track study performance in real-time
Gain comprehensive insights into study progress and identify risks with advanced reports.
- Monitor study milestones and document health in real-time
- Quickly pinpoint at-risk areas and mitigate issues with actionable reports
- Enhance visibility with document metrics, action items, and study attributes
Collaborate remotely with sites
Seamlessly connect with study sites through the eISF for efficient, remote collaboration.
- Connect with each site’s eISF for streamlined document sharing
- Perform remote monitoring and source data verification
- Collect, route, and query site documents securely within the eTMF
Drive results that matter
Mitigate Risk
Achieve a 98%+ eTMF pass rate with automated audit trails, version control, user permissions, and secure in-app redaction.
Accelerate Timelines
Cut study start-up times by up to 40% and reduce study close-out by two weeks with effortless workflow streamlining.
Increase Capacity
Save 20-30 hours weekly and boost CRA efficiency by 25x, allowing more focus on patient care and less on administrative tasks.