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