We partnered with leading academic medical centers, sponsors, hospital systems, and site networks to create an eConsent platform that is easy-to-use and minimizes risk.
We partnered with leading academic medical centers, sponsors, hospital systems, and site networks to create an eConsent platform that is easy-to-use and minimizes risk.
Why Clinical Operations Leaders Choose Florence eConsent
Engage with Intuitive Site Workflows
Florence eConsent is designed to mimic the look and flow of paper-based informed consent to make the transition easy for participants, site staff, IRBs, and sponsors.
Relax with Proven IRB and Sponsor Approval
Florence eConsent has been approved for use by major sponsors, CROs and IRBs and is now operational at leading academic centers and nationwide health systems.
Experience an Easy-to-use Participant Interface
Participants can navigate and sign their informed consent forms from any device, anywhere and access any study they are participating in.
Stay Compliant and Secure
Built-in compliance features include signature verifications, automated audit trails, version control, and user permission options. Plus, your team is supported by our extensive compliance program to help develop SOPs for going digital.
For Sponsors: Deploy eConsent Across Sites
Sponsors and CROs can easily deploy eConsent across their portfolio of sites for any study. Integration with the SiteLink™ platform gives them 24/7 visibility into consent processes.
Ensure You Always Have the Latest Versions
Easy version controls and IRB routing workflows ensure the participant is always being consented on the right informed consent version.
In clinical research, compliance is crucial. We’ve got you covered.
Overview of Florence eConsent
Overview of Florence eConsent
Intuitive Participant Management
Try intuitive workflows to get your study set up and activated fast.
Easy-to-use Participant Interface
Facilitate a participant’s experience with the consent process on a platform tested and validated by non-clinical professionals.
Global Study Management
Set up and manage consent workflows in an easy-to-use environment designed for speed and compliance.
Familiar Consent Creation
Make the transition from paper consent to electronic consent easy with a familiar workflow.
Secure Remote Access and Monitoring
Enable compliant and controlled remote access to users, including IRBs, regulatory agencies, and monitors.
We are committed to making you and your sites successful.
We are committed to making you and your sites successful.
According to user reviews, Florence is rated the #1 clinical trial workflows platform for ease-of-setup, ease-of-use and customer support.
Why being rated #1 out of 190 clinical trial platforms on G2, the peer-to-peer review site, matters for you.
“The regulatory team is very happy with the process. It gives me great pleasure to have partnered with Florence to help them be more efficient with tasks.”
Director, Research Quality and Regulatory Compliance
Multi-Site Health System
“We have staff in several different locations, so having a central access point for our information was very important and a huge draw.”
Associate Director of Research Administration
Academic Cancer Center
“We manage multi-center studies, and eBinders gives us the power to be several places at once.”
Director of Clinical Research Administration
Site Network
Florence Supports Site Enablement on a Global Scale
Florence now supports workflows between sponsors and more than 10,000 study sites in 45 countries.
