New Product Launch for Research Sites!
Automate Enrollment with Florence’s eNcounter
Contact Us ⏐ My Sponsor Uses Florence ⏐ Log In
Electronic Investigator Site File
Study Information and Password Manager
Digital Document Exchange and Remote Monitoring for Sponsors
Electronic Trial Master File
Digitize Informed Consent Workflows
Enrollment and Screening Automation
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
Make informed consent easy for you and your participants with secure, efficient, and fully digital workflows for clinical trials.
Other vendors promise eConsent solutions, but we’re the only ones that seamlessly integrate and scale with your workflow.
Intuitive
Other vendors promise simplicity, but require complex setups…Our eConsent is paper-like and intuitive—ready to use instantly.
Integrated
Other vendors promise automation, but leave you juggling platforms…Our eConsent integrates directly into your existing systems.
Scalable
Other vendors promise flexibility, but scaling is complex…Our eConsent scales effortlessly as your studies grow.
See how it works
Intuitive Participant Management
Seamless consenter workflows get your study set up and activated fast.
Easily invite participants & monitor the status of participants’ informed consent in real-time
Invite, assign, and manage study staff with pre-defined permissions
Update to latest consent versions for new protocol amendments
Distribute and track re-consenting in the same application
