Strengthen Sponsor and Site Relationships with Remote, Always-on Workflows on a Global Scale

When you partner with Florence to deploy research workflows to your sites, you give them a platform they love. Florence eBinders is ranked #1 for clinical trial workflows by sites for ease-of-use, ease-of-setup and support.

Provide study sponsors controlled and remote access to site documents and data. A single source of truth between you, sponsors, and your study sites enables transparency and speed.

CRAs with remote access capabilities can monitor over 60 sites per week with Florence. CRA staffing bottlenecks and travel costs are reduced, and CRAs can make a greater impact on study sites.

Automated workflows like electronic logs, placeholders, eSignatures and quality assurance workflows reduce start-up times by 40% for most of our customers and accelerate overall study timelines to reduce time to submission.

Over 80% of your eTMF is generated at the trial site. By integrating site workflows with your eTMF through Florence, you can exchange documents seamlessly. The eTMF pass rate of one customer increased from 65% to 98.7%.

Coupling our existing global network of connected sites with our #1-ranked site activation team, we set up your sites in days with a 92%+ site activation rate on Florence eBinders™, the industry-standard eISF and Electronic Participant Binders for sites.

Read More Customer Reviews

Activate remote site start-up, monitoring, and source data review/verification on SiteLink. Connect and deploy Florence eBinders™, the industry-standard electronic Investigator Site File and Electronic Participant Binder, on a global scale to every site in your study.

Sites are tired of sponsors forcing ill-fitting software into their workflows. As a result, sponsors rarely see the value they expect. Florence changes this by designing software for site-first workflows. And they trust us. We’re ranked #1 for clinical trial workflows by sites for ease-of-use, ease-of-setup, and support.

Today, research is conducted on a global scale, spanning borders, time zones, and regulatory agencies. Florence’s global reach – 10,000 sites in 45 countries – along with a team of regulatory experts and granular access controls enable you to deploy digital infrastructure around the world.

You benefit from the experience of a team of experts who have helped more than 10,000 clinical trial sites and 30,000 users migrate to digital workflows. This deep understanding of what makes a site successful allows us to provide the most comprehensive support in the industry.

When you establish continuous, remote workflows across many study sites around the world, you need an easy-to-use platform. With Florence, you and your sites won’t have to deal with the complex interfaces often associated with clinical software and can instead focus on getting the work done quickly.

The world’s leading academic medical centers, cancer institutes, hospitals, healthcare networks, site networks, and independent sites rely on Florence for their workflows. Through Florence, they make their workflows available to you directly.

Our expert implementation and support teams do all the heavy lifting for you to get your sites up and running, and on average we achieve 92%+ full adoption and activation rates in weeks. No matter if you’re rolling out to 50 locations or 5,000, we’ve got you covered.

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

Florence now supports workflows between sponsors and more than 10,000 study sites in 45 countries.