Differentiate Your Sponsor Offerings with Site Enablement
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 12,000 sites across 45 countries. Seamlessly integrate Florence eBinders™, the gold-standard in eISF and Electronic Participant Binder solutions, into your global study.
Why CROs Trust Florence’s Site Enablement Platform
Offer differentiated services to sponsors while reducing costs by creating a digital connection to every site in your study on a platform they already love and use in their workflows.
Increase Trust with Sponsors
Boost trust and transparency with sponsors by offering real-time insights into clinical trial site start-up processes. This innovative solution fosters collaboration and streamlines communication, ensuring efficient trials and increased sponsor confidence.
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.
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.
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.
“[With Florence’s SiteLink] we’re providing a more valuable site management experience, while allowing more time and opportunities for site support, compliance reviews and continuous monitoring of patient safety and study quality.”
Rajneesh Patil
VP of Clinical Operations and Head of Digital Strategy
IQVIA
The Site Enablement Platform
Discover how Florence’s Site Enablement Platform helps CROs offer differentiated study management to sponsors that supports enhanced site operations, strengthened site relationships, increased trust with sponsors, and accelerated clinical trials.
STUDY PLANNINGPlan for SuccessProvide a differentiator to your sponsor customers by gaining access to our searchable database of clinical research sites across 45 countries who are equipped with advanced Site Enablement Platforms. Then, pre-screen sites based on pre-filled and up-to-date feasibility profiles so you can accelerate the process and not waste time engaging with sites who don’t meet your essential criteria. Now you can choose the sites that best meet your needs, and begin your study with the greatest chance of success. |  |
SITE START-UPReduce Bottlenecks in Site Start-upOffer sponsors accelerated study start-up capabilities by activating sites remotely and equipping 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. Enable visibility to sponsor partners into site start-up processes to increase trust. |  |
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% and giving your sponsor partners controlled visibility into site operations and milestone tracking. 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, SubmittedProvide sponsors accelerated closeout timelines with improved TMF submission quality, compliance, and completeness. Integrate site documents with yours or the sponsors eTMF through automated quality control workflows, using seamless methods like API integrations, email, and drag-and-drop. Equip sites with long-term archiving included. |  |
#1
Rated #1 by sites on G2 for ease of use, ease of setup, and customer support
12k
Sites activated on the platform
45
Countries connected
92%
Site adoption rate
40%
Reduction in site workload
6.5
Million workflows per month
Make Sites Happy
(Your CRAs Will Thank You Too)
Enable Sites, Accelerate Trials
E2E Workflow Automation
Manage and automate all workflows in one place. Create, edit, sign, gather and review eISFs, eTMFs, and eBinders all within the platform.
Open Integrations
No need for sites to reinvent their workflows. We integrate with many systems, so sites can work with you while continuing to use their own custom workflows.
Site Intelligence
Gain deep insights into site operations on a global scale with the ability to zoom in on a single document at an individual site. Track compliance and performance with our reporting and analytics dashboards.