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Accelerate study operations with real-time site performance visibility and digital document distribution and exchange

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Trusted by these industry leaders around the globe

Florence is the platform powering scalable clinical operations worldwide

Simplify Documentation Management

Use templated document structures to create a consistent experience across sites, studies, and teams

Enhance Compliance

Maintain audit readiness with centralized document access and automated completion tracking

Improve Study Visibility

Monitor site performance, track progress, and maintain oversight across your entire study portfolio

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Remote Access to Every Site

Gain real-time visibility into site documentation and study activity with secure digital access for continuous oversight across every site in your portfolio

  • Always-On Document Access
  • Automated Monitoring Audit Trails
  • Task Assignment and Follow-Up

Site-Driven Document Workflows

Leverage Florence's 90%+ eISF adoption to gain real-time visibility into site documentation, reduce manual follow-up, and accelerate study oversight

  • Electronic Signatures
  • Automated Tasks and Workflows
  • Role-Based Access Controls

Simplified Remote Monitoring

Enable monitors to review documentation, collaborate with sites, and resolve issues remotely throughout the study lifecycle

  • Pre-Visit eISF Review
  • Direct Access to Redacted Participant Binders
  • Automated Visit Scheduling and Activity Tracking

Intelligent Document Exchange and TMF Filing

Automate document collection, review, and TMF filing to reduce manual effort and improve document quality

  • eTMF Synchronization
  • Automated Quality Control Reviews
  • Proactive Identification of Missing or Incomplete Documents

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 visibility control over every study with a single platform

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Sites

eBinders

Accelerate study activation with a digital ISF built for compliance

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