eBinders

Simplify study startup and activation with a digital ISF that allows for remote monitoring, document sharing, study management and compliance supervision all in one place.

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eBinders product interface preview

Trusted by these industry leaders around the globe

Florence was built with sites in mind. Streamline all the workflows that matter.

Accelerate Your Timelines

Cut study start-up times by 40% and reduce study close-out by two weeks*

Reduce Your Risk

Monitor document status in real time and ensure critical records are always inspection-ready

Increase Your Capacity

Eliminate administrative bottlenecks and free your team to focus on study selection and growth

See How It Works

Regulatory Workflows

Build audit-ready, site-controlled workflows for document creation, management, and sharing

  • Keep track of document modification with audit trails
  • Provide role-based access based on staff permissions
  • Easily request eSignatures and manage document uploads

System Administration

Leverage intuitive workflows for fast study setup and activation

  • Create standardized eISF templates and naming conventions based on your SOPs
  • Progress workflows with digital placeholders, due dates, and task assignments
  • Identify risk areas with advanced reporting and dashboards

Remote Monitoring

Work with sponsors and CROs remotely on start-up, monitoring, and source data review.

  • Empower monitors to review eISF content before on-site visits, ensuring smoother collaboration and preparation
  • Eliminate duplicate document uploads to sponsor portals with direct access to redacted participant binders
  • Automate remote visit scheduling, monitor activity tracking, and follow-up communication

Source Management

Sync source with participant binders to collect all participant source data in a single location.

  • Integrate with your CTMS and EMR/EHR system to route certified copies to participant binders
  • Built-in redaction controls ensure only authorized users see Protected Health Information (PHI)
  • Florence ePrinter enables secure, encrypted digital exchange of sensitive documents between clinical systems

Florence integrates with your existing tools

We don't replace tools, we connect them in a way that works for both sites and sponsors. Between our 90% eISF adoption rate and the 65K sites on our platform, Florence is the software of choice because it makes work seamless and cost-efficient.

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

Streamline Clinical Trials with Flexible, Compliant eISF Management

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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

Run flexible, faster, fully compliant trials with eBinder

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A Unified Platform Built for Clinical Trial Management

Florence provides a comprehensive platform for managing clinical trials from startup through closeout

Sponsors

eTMF

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

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Sites

eConsent

Accelerate study enrollment with a digital informed consent tool

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