The Fastest-Growing Trial Operations Platform
A unified platform connects teams, digitizes workflows, and delivers real-time insights to speed study startup, strengthen oversight, and keep trials inspection-ready end to end.
Clinical trials run on disconnected systems, manual processes, and fragmented communication between sponsors, CROs, and sites. The result is delayed startup, limited visibility, inconsistent oversight, and unnecessary operational risk.
Florence is the fastest-growing trial operations platform, connecting 65,000+ study sites and 600+ life science organizations worldwide. Unlike sponsor-only portals and study-specific point solutions, Florence creates a shared operational layer where sites and sponsors work together in the same system.
The result is faster study startup, real-time operational visibility, and always-on inspection readiness.
Why Clinical Operations Leaders Choose Florence
Superior Site Adoption
Most clinical trial technology struggles with site adoption. Florence is used by more than 65,000 study sites because it helps sites manage their own work, not just sponsor requirements.
When sites actively use the platform, sponsors gain visibility into trial operations without creating additional burden.
Global Operational Visibility
Monitor startup progress, document status, site activity, and study execution across your portfolio in real time.
Replace spreadsheets, status meetings, and manual follow-up with a single operational view of trial performance.
Accelerate Study Startup
Digitize document exchange, approvals, signatures, and site workflows to reduce startup delays and move studies forward faster.
Identify bottlenecks early and keep activation timelines on track.
Enable Remote Monitoring
Provide compliant access to site documentation and study records without relying on on-site visits.
Give CRAs and study teams the visibility they need while reducing monitoring burden for sites.
Operational Intelligence from Site Workflows
Florence generates intelligence from the tools sites already use every day.
Move beyond static reports and gain insight into site activity, document readiness, workflow completion, and operational risk.
Always-On Inspection Readiness
Automated audit trails, version control, permission management, and complete document histories help maintain compliance throughout the study lifecycle.
Support regulatory inspections with confidence.
Built for the Clinical Trial Ecosystem
Florence works alongside your existing clinical systems, including CTMS, eTMF, and other operational platforms.
Instead of replacing your ecosystem, Florence connects it to the sites where trial work actually happens.
Get the Full Trial Operations Platform Overview