Florence’s eConsent

Stop Chasing Paper Consent Forms. Florence eConsent eliminates consenting chaos by embedding digital workflows directly into the platform that 65,000+ sites already use. Get flexible consent options, real-time visibility, and audit-ready data integrity without burdening sites with another disconnected system.

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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 team stays compliant without the scramble.

Easy To Use

Remote, in-person, or paper, Florence eConsent meets participants where they are. Simple enough for participants to complete independently and powerful enough for coordinators to manage every consent in 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.

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

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 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

  • 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

Integrate with the tools you use every day.

In clinical research, compliance is crucial. We’ve got you covered globally.

Let’s Cure Clinical Trials Together