Electronic Informed Consent For Clinical Research

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.

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. Participants can navigate and sign their informed consent forms from any device, anywhere, and access any study they are participating in.