eConsent

Deliver a seamless informed consent experience for participants and study teams with secure, fully digital workflows

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eConsent product interface preview

Trusted by these industry leaders around the globe

Florence provides the foundation for scalable, compliant clinical operations

Enhance Participant Engagement

Create an accessible experience that improves participation and retention

Increase Enrollment Efficiency

Reduce administrative burden and accelerate participant enrollment

Reduce Compliance Risk

Standardize consent processes and maintain regulatory readiness

See How It Works

Accelerate Participant Enrollment

Launch studies faster with streamlined participant consent workflows

  • Invite participants and track consent status in real time
  • Automatically manage protocol amendments and consent updates
  • Distribute and track re-consent from a single platform

Easy-to-Use Participant Interface

Enable a frictionless, participant-friendly consent experience

  • Support remote and on-site consent across any device
  • Verify participant identity remotely
  • Give participants one login for all active studies

Global Study Management

Manage consent workflows at scale while maintaining compliance

  • Monitor and countersign consent forms with ease
  • Access eConsent directly through Florence eBinders
  • Maintain compliance with audit trails, version control, and signature verification

Secure Remote Access & Monitoring

Provide compliant access to study stakeholders without added burden

  • Give monitors remote access to consent and regulatory documents
  • Support compliant review by IRBs and regulatory agencies
  • Capture regulated activity with comprehensive audit trails

Connect the Systems Powering Your Clinical Trials

Florence works alongside your existing technology investments, bridging sponsors, CROs, and sites through a unified workflow. With 90% eISF adoption and a network of 65,000+ sites, Florence helps organizations improve efficiency without disrupting established processes.

Florence connects research sites and sponsors/CROs into one eClinical ecosystem

Accelerate Trial Execution Without Compromising Compliance

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Real Stories, Real Success

Capterra and G2 ratings

Trusted by clinical research teams on Capterra and G2.

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65K study sites across 90+ countries run their trials with Florence

Globally compliant clinical trial software

Accelerate Clinical Trials Without Compromising Compliance

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A Unified Platform Built for Clinical Trial Management

Florence's suite of tools is built for end-to-end trial needs

Sponsors

eTMF

Gain complete visibility and control across every study from a single dashboard

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Sites

eBinders

Accelerate study activation with a digital ISF built for compliance

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