Why Trust Florence for your Clinical Trial Workflows
Remotely Links Sites and Sponsors
Always-on, remote digital document and administrative workflows transform the way sponsors, CROs and sites work together in traditional site-based and decentralized trials.
Makes Site Staff Happier
Study sites rate Florence #1 for ease of use, setup, and support. If you’re a site leader giving your team eBinders or a sponsor/CRO deploying eBinders to your sites, you can count on them loving it.
Maximizes Employee Productivity
Linked workflows improve employee efficiency and productivity. Reduce the impact of hiring and retention challenges. CRAs on Florence can monitor 60+ sites per week.
Expands Patient Access
Remote links with study sites in historically underserved areas increase access to diverse participant populations. Florence’s network of 10,000 connected study sites is already within 25 miles of 80% of the US population and in 45 countries worldwide.
Accelerates Study Timelines
Standardizing processes while still enabling flexibility to adapt to individual site processes helps increase efficiency and accelerate timelines. Florence’s solutions reduce study start-up times by 40% in most instances.
Increases Safety and Compliance
Audit trails, version controls, controlled user access, and built-in PHI redaction take the risk out of going digital. Adverse events workflows and electronic consenting coupled with real-time remote site monitoring improve participant safety.
Florence’s platform is helping Pfizer 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
Pfizer
According to user reviews, Florence is rated the #1 clinical trial workflows platform for ease-of-setup, ease-of-use and customer support.
Why being rated #1 out of 190 clinical trial platforms on G2, the peer-to-peer review site, matters for you.
High Adoption: We lead the industry with 92%+ site technology activation per study.
Faster Timelines: Intuitive workflows that eliminate duplicate work mean work gets done fast.
Low FTE Burden: You don’t need large dedicated IT teams to support implementation and management.
Always Reliable: Our customers have had 100% uptime over the last 12 months. We’re there when you need us.
In clinical research, compliance is crucial. We’ve got you covered.
Florence’s Research Workflow Products
“Our eTMF QA score went from a 65% submission pass rate to 98.7% by having real-time remote access to the site eISF.”
Aperio Clinical Outcomes
“92% of 140 study sites in 8 countries were activated on Florence for remote source access and monitoring in four weeks.”
VP Clin Ops, Top 3 Pharma
“Our highest performing CRAs are now ‘visiting’ 64 sites per week with remote monitoring on Florence, up from 2 per week.”
VP Clin Ops, Top 3 Global CRO
Florence Supports Remote Workflows on a Global Scale
Florence now supports workflows between sponsors and more than 10,000 study sites in 45 countries.
We are committed to making you and your sites successful.
We are committed to making you and your sites successful.
We love working with sponsors on Florence. Collaborating in real-time on a single document management platform helps us tackle study tasks faster and keep research on track.
Dr. Christina Brennan
VP of Clinical Research