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Electronic Investigator Site File
Enrollment and Screening Automation
Study Information and Password Manager
Digitize Informed Consent Workflows
Document Exchange + Remote Monitoring
Electronic Trial Master File
StudyReady Participant Database
Get an inside look at how the top rated Site Enablement Platform can transform your operations first-hand. Book a demo now.
Discover how the Florence Platform supports pharma and biotech companies
Discover how the Florence Platform supports Contract Research Organizations
Discover how the Florence Platform supports clinical research sites and networks
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
Unleashing the Next Era of Clinical Trial Intelligence
Florence Trial Operations Platform
How Florence Transforms Operations For:
Florence is the #1 rated platform for research sites to digitize and automate their research workflows.
Digitize every document and automate workflows to centralize data, accelerate operations, and boost team capacity.
Maintain compliant audit trails, control access with role-based management, and streamline electronic signatures.
Enable remote monitoring and document collaboration to improve communication and accelerate trial operations.
Leverage intuitive eConsent for quick in-person or remote consenting, reducing risks and speeding up enrollment.
Florence is the trusted platform for sponsors and CROs to digitize every research site in their study and automate operational workflows.
Unify document management and exchange across all sites, regardless of their internal workflows.
Accelerate studies with seamless document distribution, management and automated eTMF syncing.
Boost efficiency by remotely accessing site documents and source data, expanding CRA capacity.
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
Digitize, automate, and integrate your investigator site files, participant binders, and logs – while providing remote monitoring for sponsors and CROs.
Make informed consent easy for you and your participants with secure, efficient, and fully digital workflows for clinical trials.
Transform your enrollment process with the solution that centralizes, automates, and optimizes every participant journey.
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
Effortlessly distribute, monitor, and exchange study documents with every site—wherever they work, whenever they need it.
Maintain a StudyReady™ database of study candidates to match with future studies and route directly to sites.
The only eTMF built for ease-of-use and direct connectivity to study sites for eISF document exchange.
Global Visibility.
65k
Study Sites
600+
Sponsors Supported
90+
Countries
In clinical research, compliance is crucial. We’ve got you covered globally.
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