The leading eRegulatory and eSource platform trusted by 5,000+ Clinical Research Sites

Accelerate your research with Florence eBinders™. Secure. Compliant. Easy-to-use. Flexible.

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“Florence stood out amoung vendors for two things: Florence is easy for Principal Investigators to use, and the Florence team made adoption and onboarding simple. Our team loves the platform!”

Dawn East
VP of Research

Join 5,000+ clinical trial sites scaling capacity and accelerating research with Florence eBinders™.

Eliminate inefficient document workflows wasting time and money, limiting your ability to scale and attract new studies.

Florence eBinders integrates all of your clinical trial systems, automates regulatory processes, reduces contract negotiation time, tracks study progress, and enables secure remote monitoring.

Join our growing network of over 5,000 research teams.

eRegulatory Testimonial

“We manage multicenter studies and eBinders gives us the power to be several places at once. It works really well for remote regulatory document review and enrollment approvals, and as a result gets sites up and running quickly.”

Ashely Friend
Clinical Trials Manager

Florence eBinders™ | See what’s inside

 Clear insights into what needs to be done

  • Global view of all of your studies in one place.
  • Actionable tasks to keep you on track.
  • No more losing documents or forgetting deadlines.
  • Easy-to-use and flexible for your entire team.
Florence eBinders Overview 
 Fully compliant, easy-to-use, eSignatures

  • Signing documents is a breeze with our eSignature tool.
  • Actionable workflows that eliminate repetitive tasks like requesting signatures, notifying users, and chasing down documents.
  • Intuitive “sign and go to next” feature enables easy step-by-step process for signing documents.
  • Fully compliant and accepted by regulatory bodies and sponsors.
eSignatures Part 11 Compliant 
 Project management tools accelerate study startup and progress 

  • Know where all your studies are and which ones are off track.
  • Easy visibility into multi-site studies.
  • Stay on track with study startup and anticipate potential delays.
  • Uncover bottlenecks and reduce barriers to startup.
Study Startup Project Management 
 Enable true remote monitoring with audit trails

  • Full document and binder audit trails track views and changes.
  • Grant remote access to sponsors, IRBs and regulatory bodies.
  • Seamlessly manage how and when monitors can access particular binders and documents.
  • Easily and automatically redact parts of files and binders.
Audit Trails and Remote Monitoring 
 Eliminate redundant processes with complete system integration

  • Connect with CTMS, EMR, eTMF, Email, and other tools you use.
  • Edit documents directly inside of eBinders™.
  • Eliminate manual transfer of source documents with instantaneous uploads into a regulatory eBinder.
  • Streamline communication with your CTMS saving you valuable time and reducing the risk of compliance errors.
  • Forward emails directly into the appropriate site/study binders.
Integration Florence eBinders Editor 

What’s Next?

Learn what adding eRegulatory looks like.

Download our free Roadmap to eRegulatory guide developed with tips and best practices from over 2,000 successful research site, sponsor, and CRO implementations.

Download Free Guide

Discover how Florence eBinders™ fits with your team.

Setup a few minutes to chat with our team and let us help you discover how eRegulatory best fits with your site, plus get an inside look at Florence eBinders™.

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