Digitize Every Site. Automate Every Workflow. Accelerate Every Study.

Trusted by hundreds of sponsors, CROs, and over 37,000 sites across 90 countries to digitize workflows and intelligently automate:

  • Feasibility & site selection

  • Study start-up & document management

  • Patient enrollment & remote monitoring

See How Sponsors Can Ensure Their Sites Are Aligned with ICH E6 R3

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.

Collaborating Globally to Transform Research

Florence’s Site Orchestration 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.

Accelerate Your Clinical Trials

Global presence

37k

Sites

90+

Countries

7.2M

Monthly workflows

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

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