Florence eConsent Product Tour 

Stop Chasing Paper Consent Forms

Florence eConsent eliminates consenting chaos by embedding digital workflows directly into the platform 65,000+ study sites already use. Get flexible consent options, real-time visibility, and compliant eSignatures with a full audit trail, without burdening sites with another disconnected system.

Explore key features including:

  • Remote, in-person, and paper consent workflows in one platform
  • Real-time consent status monitoring across your portfolio
  • CRA remote access to consent documentation
  • Drag-and-drop consent builder with live previews

Take the tour now and see how eConsent fits into your existing clinical research workflow instead of creating another system to manage.

5k+

Template forms updated and reused across studies.

831+

Studies within Florence eConsent.

37k+

Study participants successfully navigating the platform.

Built-in Compliance

Florence eConsent preserves IRB-approved documents, enforces automated version control, and delivers inspection-ready audit trails in real time so your clinical research team stays compliant without the scramble.

Built for Participants

Rated 5 stars by the teams who use it daily. Remote, in-person, or paper, participants complete consent independently, and coordinators manage every consent from one place.

Integrated workflows

Florence eConsent runs natively on the platform 65,000+ sites already use. The built-in eBinder integration keeps consents, documents, and workflows connected, eliminating duplication and maintaining complete operational control.

See how it works

Flexible Workflows for Faster Enrollment

Expand your enrollment population without opening new sites or adding new systems and keep patients engaged

  • Support remote, in-person, and paper consent workflows in one platform

  • Invite participants and monitor consent status in real time

  • Handle protocol amendments and track re-consenting in the same application

  • Give participants 24/7 portal access to review forms on their own time

Flexible Workflows and a 24/7 participant dashboard for faster enrollment
Remote Monitoring to Cut Costs

Remote Monitoring to Cut Costs

Eliminate unnecessary site visits and reduce monitoring overhead without sacrificing oversight

  • Give CRAs and CRO teams remote access to consent documentation in real time

  • Monitor consent status across your studies or portfolio through centralized dashboards

  • Access inspection-ready audit trails that capture all regulated activity

  • Reduce travel costs while maintaining compliance and control

Compliance Built-In to Lower Risk

Reduce regulatory exposure with automated version control and inspection-ready audit trails that satisfy FDA and global regulatory requirements

  • Preserve IRB-approved documents in their original state

  • Enforce automated version control and tracking across all sites

  • Maintain complete audit trails that capture all regulated activity

  • Native integration with Florence eBinders means one login, one system

Compliance Built-In to Lower Risk
eConsent in-app form builder

Build & Manage Consent Forms In-App

Respond to protocol amendments faster without waiting on vendors or rebuilding workflows

  • Create fillable consent forms with drag-and-drop builder.  Eliminate use of custom Adobe or pdf workarounds

  • Update consent forms in real time with live preview

  • Support multiple signers and multilingual forms

  • Reuse template forms across studies to maintain consistency

Discover how eConsent reduces risk, speeds enrollment, and cuts operational costs.

Integrate with the tools you use every day

Built for ICH GCP E6(R3) and the regulatory standards your studies run under

Let’s Cure Clinical Trials Together