Collaborate
With Any Site.

Anywhere, Anytime.

Florence’s Site Enablement Platform brings sponsor-site collaboration to life. By designing a platform around sites’ needs and enabling them to do their best work, Florence frees clinical trials from bottlenecks, so they can accelerate and scale.

Collaborate
With Any Site.

Anywhere, Anytime.

Florence’s Site Enablement Platform brings sponsor-site collaboration to life. By designing a platform around sites’ needs and enabling them to do their best work, Florence frees clinical trials from bottlenecks, so they can accelerate and scale.

It’s Time to Cure the Chaos

Sites are drowning under the demands of today’s clinical research trials, slowing clinical trials, increasing costs, and delaying cures.

62%

Of the research site capacity actually exists to meet patient enrollment targets

78%

More companies have active pipelines than 10 years ago

53%

More clinical trials start every year than a decade ago

41%

Of clinical trials now target complex therapies adding pressure to site operations

Your digital solutions may work for you, but forcing them on sites is a prescription for failure. Duplicate workflows, learning curves, and clunky integrations crush your sites’ progress and keep your discoveries from the patients who need them.

But what if you could enable every site to do their best work?

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.

STUDY PLANNING

Plan for Success

Search for sites to participate in your study in our Site Navigator Network, linking 18,000+ sites in 55+ countries. Identify the ideal sites for your study.

Then, review their pre-filled feasibility profiles to ensure they meet basic criteria while getting a jump start on launching your study in Florence’s Site Enablement Platform. Now you can choose the sites that best meet your needs, and begin your study with the greatest chance of success.
For Sponsors
For CROs
For Sites

SITE START-UP

Reduce Bottlenecks in Site Start-up

Activate 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.
For Sponsors
For CROs
For Sites

SITE CONDUCT

Simplify FPI to LPO

Digitize 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.
For Sponsors
For CROs
For Sites

SITE CLOSE-OUT

Signed, Sealed, Submitted

Close out your studies on time with improved TMF submission quality, compliance, and completeness.

Integrate site documents with the eTMF through automated quality control workflows, using seamless methods like API integrations, email, and drag-and-drop. Equip sites with long-term archiving included.

For Sponsors
For CROs
For Sites

#1

Rated #1 by sites on G2 for ease of use, ease of setup, and customer support

18k+

Sites activated on the platform

55+

Countries connected

92%

Site adoption rate

40%

Reduction in site workload