Florence’s 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.
Proven IRB and Sponsor Approval
Florence’s eConsent has been approved for use by major sponsors, CROs and IRBs and is now operational at leading academic centers and nationwide health systems.
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.
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.
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.
Always Up-to-date 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.