Florence’s eConsent

Make informed consent easy for you and your participants with secure, efficient, and fully digital workflows for clinical trials.

Other vendors promise eConsent solutions, but we’re the only ones that seamlessly integrate and scale with your workflow.

Intuitive

Other vendors promise simplicity, but require complex setups…Our eConsent is paper-like and intuitive—ready to use instantly.

Integrated

Other vendors promise automation, but leave you juggling platforms…Our eConsent integrates directly into your existing systems.

Scalable

Other vendors promise flexibility, but scaling is complex…Our eConsent scales effortlessly as your studies grow.

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

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