Connect to and Enable Every Site
Accelerate timelines. Increase site capacity. Reduce site burden.
Identify and pre-screen sites for your study with ease. Streamline remote site start-up, monitoring, and source data verification for every location.
Boost site performance and become the preferred sponsor by utilizing leading eISF and eConsent platforms trusted by 18,000+ sites across 55+ countries. Seamlessly integrate Florence eBinders™, the gold-standard in eISF and Electronic Participant Binder solutions, into your global study.
Why Sponsors Trust Florence’s Site Enablement Platform
The site-trusted solution for connecting workflows and streamlining clinical trial operations on a global scale.
Increase Site Satisfaction
Empower your sites with Florence eBinders via SiteLink, the top-rated platform for clinical trial workflows, acclaimed for its user-friendliness, effortless setup, and exceptional support.
Accelerate Study Start-up
Accelerate your drug development process with our automated workflows. Cut start-up times by 40% and reduce study timelines, all while streamlining your workflow.
Decrease Site Workloads
By providing your sites with eBinders, you equip them with a workflow engine that streamlines redundant workflows and consolidates divergent procedures, leading to a reduction of site workloads by as much as 40%.
Expand Patient Access
Embrace the power of digital connectivity and work with any site, anywhere. By deploying remote digital workflows, you can effortlessly expand your network and collaborate with geographically dispersed sites, enabling you to conduct research with greater ease and efficiency.
Maximize CRA Efficiency
Empower your CRAs with remote access capabilities. SiteLink allows for remote monitoring of over 60 sites per week, reducing staffing bottlenecks and travel costs while increasing impact on study sites.
Improve TMF Quality
Integrate SiteLink with your eTMF for seamless document exchange with sites. Boost your eTMF pass rate from 65% to 98.7% like one of our satisfied customers.
“Florence’s platform is helping Pfizer to respond to the changing environment … and further progress 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
Pfizer
The Site Enablement Platform
Introducing the Site Enablement Platform for Clinical Trial Sponsors. Our name is almost as long as your trials, and its our job to change that. Florence is designed for what sites need in order to deliver what you need.
SITE START-UPReduce Bottlenecks in Site Start-upActivate sites remotely and equip sites with digital workflows that integrate with their existing workflows. Deploy the #1 rated eISF platform to sites to enable study start-up document routing and real-time collaboration in just a few clicks. Monitor performance and activity across all sites in a single location. |  |
SITE CONDUCTSimplify FPI to LPODigitize and integrate every document workflow from first-patient-in to last-patient-out, reducing site burden by up to 40%. Enable sites with the best-in-class eISF (eBinders) and eConsent platform to streamline their operations while activating always-on remote monitoring capabilities, advanced site performance insights, and real-time document exchange with the eTMF. |  |
SITE CLOSE-OUTSigned, Sealed, SubmittedClose out your studies on time with improved TMF submission quality, compliance, and completeness.</ |