Florence Trial Operations Platform

Unleashing the next era of clinical trials intelligence.
Florence powers shared workflows and AI-augmented automation across sites and sponsors.

  • Expedite startup: No Silos, no paper, no delays

  • Reduce risk: Be inspection and audit ready; anytime

  • Save millions with digitization and remote monitoring

The 2026 State of Clinical Trial Technology Report

Florence Trial Operations Platform

How Florence Transforms Operations For:

Research Sites

Florence is the #1 rated platform for research sites to digitize and automate their research workflows.

Intelligent Study Workflows

Digitize every document and automate workflows to centralize data, accelerate operations, and boost team capacity.

Automated Compliance

Maintain compliant audit trails, control access with role-based management, and streamline electronic signatures.

Connect with Sponsors

Enable remote monitoring and document collaboration to improve communication and accelerate trial operations.

Simplify Patient Consenting

Leverage intuitive eConsent for quick in-person or remote consenting, reducing risks and speeding up enrollment.

Sponsors + CROs

Florence is the trusted platform for sponsors and CROs to digitize every research site in their study and automate operational workflows.

Standardize Site Operations

Unify document management and exchange across all sites, regardless of their internal workflows.

Digitize Study Start-up & Close-Out

Accelerate studies with seamless document distribution, management and automated eTMF syncing.

Activate Remote Monitoring

Boost efficiency by remotely accessing site documents and source data, expanding CRA capacity.

Enable Sites with Top-Rated Software

Provide Florence’s #1 rated eBinders document automation solution to streamline workflows and mitigate risks globally.

Site made. Sponsor trusted.

Florence’s Trial Operations Platform

Research Site Solutions

Florence’s eBinders™

Digitize, automate, and integrate your investigator site files, participant binders, and logs – while providing remote monitoring for sponsors and CROs.

Florence’s eConsent

Make informed consent easy for you and your participants with secure, efficient, and fully digital workflows for clinical trials.

Florence’s eNcounter™

Transform your enrollment process with the solution that centralizes, automates, and optimizes every participant journey.

Florence’s StudyOrganizer™

Access your study bookmarks, passwords, and contacts in one place on our FREE and easy-to-use study organizer for busy research sites.

Sponsor+CRO Solutions

Florence’s SiteLink®

Effortlessly distribute, monitor, and exchange study documents with every site—wherever they work, whenever they need it.

Florence’s ParticipantLink™

Maintain a StudyReady™ database of study candidates to match with future studies and route directly to sites.

Florence’s eTMF

The only eTMF built for ease-of-use and direct connectivity to study sites for eISF document exchange.

Start Faster, Operate with Intelligence

Global Visibility.

65k

Study Sites

600+

Sponsors Supported

90+

Countries

In clinical research, compliance is crucial. We’ve got you covered globally.

What’s New