How Florence’s eConsent Transforms Your Operations
Digitize, automate, and integrate your consent process.
Intuitive Site Workflows
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.
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.
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.
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.
Consent On-Site, Without the Paper
For those who would rather provide consent in person, sites can explain ICF to the participant—as well as their LARs, parents, or guardians—then hand over a tablet to capture a stylus signature on an electronic form.
Stay Connected to eBinders
Share ICFs from eConsent directly to eBinders, saving time and ensuring completed forms are being stored in the correct folder.
In clinical research, compliance is crucial. We’ve got you covered.
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Intuitive Participant Management
Try intuitive workflows to get your study set up and activated fast.
![Invite Participants_2_800x600 Invite participants product screenshot in computer screen](https://sp-ao.shortpixel.ai/client/to_webp,q_glossy,ret_img,w_600,h_450/https://florencehc.com/wp-content/uploads/Invite-Participants_2_800x600-600x450.png)
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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.
![Global Study Manager_computer_800x600 Global Study Manager screenshot on a computer screen](https://sp-ao.shortpixel.ai/client/to_webp,q_glossy,ret_img,w_600,h_450/https://florencehc.com/wp-content/uploads/Global-Study-Manager_computer_800x600-600x450.png)
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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.
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