The Site Enablement Platform for Sponsors

Discover how Florence’s Site Enablement Platform helps sponsors support site operations, strengthen site relationships, and accelerate clinical trials.

Site Conduct

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.

How Florence Streamlines Site Conduct

Enable continuous digital collaboration with every study site for the complete study life-cycle including remote monitoring and remote source data verification and review.

Gain 24/7 Visibility Into Every Site

Because every site maintains their complete eISF on a connected platform you gain real-time visibility into all operations including document status, tasks, and other integrated workflows.

Ensure Site Adoption

Research sites love using Florence, ranking eBinders the #1 platform for ease-of-use and quality of support out of 190 vendors. This means sites adopt the platform (95%+ average adoption) and use it for the end-to-end management of your study, so you never have to worry about disrupting site workflows.

Activate Remote Monitoring

Provide your CRAs with a complete remote monitoring experience that integrates directly with the sites workflow. Most sponsors reduce their on-site visits by over 50%, cutting travel costs, maximizing CRA efficiency, and enabling a continuous monitoring posture.

Enable Remote Source Data Review

A simple front-end integration to the sites existing EMR/EHR or other eSource platform, coupled with easy-to-use paper source capture tools, allows your CRAs to seamlessly conduct source data review and verification remotely without disrupting the site workflows.

Maintain Inspection Readiness

Know the status of every document at every site in real-time across your entire study, while enabling the ability to drill down to a specific document and assign remediation tasks to the site.

Gain Visibility into CRO Operations

When outsourcing monitoring and site management to a CRO Florence’s Site Enablement Platform gives you real-time visibility into their operations so you can ensure you remain a sponsor of choice at your study sites.

Work Seamlessly with Frontier Sites

Working with new to research sites that are geographically dispersed without worry about compliance issues and operational blindspots because you gain 24/7 visibility directly into their operations.

Increase CRA Productivity

Remote monitoring directly integrated with the sites workflows allow most CRAs to monitor and manage 2x more sites than traditional methods, helping your organization scale your studies without increasing staff.

“[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

An Inside Look at Managing Site Conduct with Florence

Start-up Sites Remotely

Remotely activate and start-up your study sites with a complete suite of electronic binder solutions.

  • Deploy the industry-standard electronic Investigator Site File (eISF) to every site with templates and pre-built workflows.

  • Distribute fully electronic Participant Binders to study sites.

  • Create and track placeholders, due dates and task assignments to keep studies progressing.