Transform your clinical trial operations with remote access to all of your study sites in a single place.

Florence connects Sponsors and CROs directly to the #1 eISF workspace installed at 10,000 Investigator sites across 44 countries. Plus, we get your other study sites connected fast – and we do it for you.

On-Demand Demo
Whitepaper Download

Join leading sponsors and CROs using Florence eHub to turn on remote access to their study sites.

Built on the digitally connected network of 10,000+ Investigators managing their eISF in Florence eBinders, Florence eHub provides sponsors and CROs real-time site access, advanced remote monitoring capabilities, automated start-up activation, and eTMF document exchange.

Watch On-Demand Demo
Blue Quote Box

Florence’s platform is helping us to respond to the changing environment due to COVID-19 and further progress COVID-19 research with the capability to perform remote monitoring where approved by regulatory authorities and ethics committees.

Rob Goodwin
VP and Head of Operations in Global Product Development

Established Global eISF + Remote Site Access Network

Study Sites
Monthly Monitoring Actions

How does Florence eHub work?

eHUB Publisher

Integrate your eTMF with Site eISFs

Eliminate the need for mailing, emailing, and faxing study documents, and legacy site upload portals, by directly integrating your eTMF with your sites eISF

  • Deploy a fully functioning Electronic Investigator Site File (eISF) to all sites

  • Publish eTMF file structures directly into Florence eHub, a secure and compliant eISF workspace for sites.

  • Exchange documents with a single site, or all of your sites, in one click.

  • Fully compliant for the site and the sponsor with granular access controls

Enable Real-Time Site Oversight

Comply with GCP IH6 V2 requirements for site oversight

  • Be alerted of potential compliance risks earlier

  • Track study startup against predetermined milestones

  • Communicate with sites directly and access study documents instantly

Florence eHub - Clinical Trial Site Oversight
Florence eHub - Clinical Trial Site Oversight 2

Forecast Site Performance

Know where all of your sites stand with their startup and study progress in real-time.

  • Analyze historical site operational performance to forecast feasibility

  • Forecast study startup time based on site historical performance

  • Understand the mind-share your study is receiving at sites

  • Remain aware of site inspection readiness

Keep Sites on Track

Easily give CRAs the ability to assign tasks and specify deadlines for sites.

  • Assign tasks to each individual site or across the study.

  • Build project timelines delivering actionable insights into startup progress.

  • Sites notified of required documents in real-time.