Florence eBinders™

Join the 37,000+ sites that have moved to the #1 electronic Investigator Site File (eISF) for automated workflows and the digital connectivity essential for collaborating with sponsors and CROs.

Regulatory Features

Role Based Access

Version Control

Audit Trails

Part-11 eSignatures

Benefits of Using Florence eBinders

A compliant electronic version of your eISF

  • Simplified Regulatory Document Management

Transition from paper-based ISFs to a site-controlled, web-based system for effortless creation, management, and sharing of essential regulatory documents.

  • Remote Monitoring

Empower monitors with remote access to review eISF content before on-site visits, facilitating smoother collaboration and preparation.

  • Streamlined Workflows and Signatures

Benefit from automated workflows and electronic signature capabilities, fostering efficiency and compliance in document handling processes.

Accelerate Timelines

Effortlessly streamline workflows, reducing study start-up times by up to 40%.

Increase Capacity

Save 20-30 hours weekly, allowing more focus on patient care and less on administrative tasks.

Mitigate Risk

Stay inspection-ready with automated audit trails, version control, user permissions, and secure in-app redaction.

User-Friendly

Rated #1 on G2 for ease of use, setup, and support for three consecutive years.

In clinical research, compliance is crucial. We’ve got you covered.

Why being rated #1 out of 190 clinical trial platforms on G2 by research sites matters for you.

  • High Adoption: We lead the industry with 92%+ site technology activation per study.

  • Ease & Efficiency: Designed to be the most user-friendly eISF, automated workflows and intuitive search optimize document management, eliminating paper binder complexities.

  • Low FTE Burden: You don’t need large dedicated IT teams to support implementation and management.

  • Always Reliable: With a best-in-class customer satisfaction rate of 97.6% and backed by 24/7 support and online resources, we’re there when you need us.

Read More Customer Reviews

Resources

Guide

The Complete Guide to eRegulatory and eSource in Clinical Trials

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Guide

The Complete eRegulatory Evaluation Checklist

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Guide

The Complete eConsent Evaluation Checklist

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Schedule time with a Site Enablement Expert to see how Florence can make your trials more efficient.