During the month of May, we are celebrating clinical research professionals. See and vote on the inspiring stories and nominate a clinical research professional for The Florence Effect award. Nominations and voting are now open!
Transform your Clinical Trials with the
#1 Platform for Electronic Document Workflow Management
Learn why Florence is the industry standard with over
6,200 research sites, sponsors, and CROs collaborating on it’s network.
Florence eBinders
Research Sites, transform your document workflows with the #1 eISF, eRegulatory, and eSource solution available.
Florence eTMF
Sponsors + CROs, transform your Trial Master File with the only eTMF digitally connected to 6,200 research sites.
Florence eHub
Sponsors + CROs, transform your eTMF quality and completeness by digitally connecting to your study site’s eISF.
Florence advances clinical trials through software for managing document and data flow between research sites and sponsors. Florence eBinders is trusted by 6,200+ Investigators to manage eRegulatory/eSource for over 1,200 studies, Florence eTMF is the most flexible eTMF on the market with a wide range of innovative features, and Florence eHub is revolutionizing site-sponsor collaboration by connecting the eTMF directly to the eISF to maximize TMF completeness and quality.
25% Faster Startup Time
Part-11 and HIPAA Compliant
Easy-to-use Interface
Flexible Workflows
Extensive Software Integrations
40% Reduced Document Cycle Time
Intuitive Site-Sponsor Connectivity
Robust Training
Custom SOPs
Proven Return on Investment
Advancing Research Together with Over
6,200 Sites, Sponsors and CROs
“We manage multicenter studies and eBinders gives us the power to be several places at once. It works really well for remote regulatory document review and enrollment approvals, and as a result, gets sites up and running quickly.”
Ashley Friend
Clinical Trials Manager
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