Florence at ACRP Annual Meeting

Visit Florence at the ACRP Annual Meeting | Booth 303

Discover why over 2,000 leading clinical trial teams trust Florence eBinders as their eRegulatory and eSource solution – and why leading sponsors are now turning to Florence eHub for site connectivity. Schedule an in-person demo at the conference.

Are you headed to the ACRP Annual Meeting in Washington D.C.? We’d love to introduce you to how Florence is changing regulatory, source, and contract management for sites and sponsors.

Stop wasting valuable time managing paper regulatory files, source documents, faxing, scanning, chasing signatures, mailing files, tracking logs, and doing something other than what you love.

Schedule an In Person Demo

ACRP Annual Meeting Resource Downloads

Part-11 Compliance Checklist
eBinders Capability Checklist
Part-11 Compliant eSignatures

I’M A SITE

Discover how the easiest-to-use and most flexible solution for eRegulatory, eSource, and Contract Management is advancing research for research sites.

Site Solutions

I’M A SPONSOR

Discover how sponsors are gaining real-time access to sites, accelerating startup, achieving real-time remote monitoring, and enabling quality control.

Sponsor Solutions
 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 
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

2018-04-20T09:57:08+00:00