Florence’s eConsent

Modern Informed Consent. Without the Friction. Digitize, manage, and monitor informed consent in one secure, compliant workflow that accelerates study startup and simplifies re-consenting.

Most solutions burden sites with another system. Florence embeds consent into existing workflows, eliminating re consent chaos and inspection risk.

Intuitive

Built around how you already consent patients, Florence removes portal friction and reduces participant drop off rates.

Integrated

Consent stays connected to your trial workflows, giving you real time visibility and maintaining inspection readiness without duplicate tracking.

Scalable

Amendments and re-consenting stay in one compliant workflow, avoiding version chaos and protecting study timelines as you scale.

Discover how eConsent simplifies and accelerates your enrollment.

See how it works

Intuitive Participant Management

Seamless consenter workflows get your study set up and activated fast.

  • Easily invite participants & monitor the status of participants’ informed consent in real-time

  • Invite, assign, and manage study staff with pre-defined permissions

  • Update to latest consent versions for new protocol amendments

  • Distribute and track re-consenting in the same application

Easy-to-Use Participant Interface

Facilitate a participant’s experience with the consent process on a platform tested and validated by non-clinical professionals.

  • Participants can consent anywhere, anytime on any platform, on-site or remotely

  • Enable remote participant identity verification

  • Single participant login and interface for all active studies they’re in

Global Study Management

Set up and manage consent workflows in an easy-to-use environment designed for speed and compliance.

  • Ensure compliance with global regulations through comprehensive audit trails, signature verifications, and version control tracking

  • Easily monitor and countersign eConsent

  • Set up repeatable and scalable processes for future studies

  • Use integrated SSO access with the Florence eBinders platform

Secure Remote Access & Monitoring

Enable compliant and controlled remote access to users, including IRBs, regulatory agencies, and monitors.

  • Provide CRAs and monitors remote access to consenting and regulatory documents, saving you time before and during monitoring visits

  • IRBs and other agencies can access consent forms compliantly

  • Audit trails capture regulated activity across the platform

Integrate with the tools you use every day.

Drive results that matter

Accelerate Enrollment

With digital-first capabilities, consent participants anywhere, anytime.

Minimize Deviations

Increase participant comprehension of protocol and consent by letting them review forms on their own time.

Eliminate Redundancies

Integrate with other software applications to eliminate duplicate work, increasing your time to focus on participants.

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

Let’s Cure Clinical Trials Together