Why Clinical Operations Teams Move to Electronic Log Workflows with Florence
Customize for Any Log Type
Digitize every log in your workflow. We support Delegation of Authority Logs, Screening and Enrollment Logs, Consent Version Logs, Communications Logs, Training Logs, Adverse Event Logs, and more.
Standardize Logs
Study-specific customization and a “living log” feature enable seamless adaptability to protocols, research teams, DOA changes, and log types.
Improve Quality and Timeliness
Eliminate illegible signatures, misplaced documents, multiple versions, expired versions and other compliance risks paper logs introduce.
Accelerate Study Timelines
Route electronic logs for completion and electronic signature in order and remotely. Assign tasks to study members and track progress. Top sites reduce start-up by more than 40%.
Enable Remote Monitoring
Enable compliant and secure remote access to all study logs while protecting PHI. Set up monitoring windows, track monitor activity, and collaborate with monitors in-app on needed actions.
Automate Compliance
Automated audit trails, extensive security controls, unlimited version controls and built-in redaction capabilities improve compliance across your organization.
In clinical research, compliance is crucial. We’ve got you covered.
See Electronic Logs on Florence in Action
Florence now supports workflows between sponsors and more than 10,000 study sites in 44 countries.
We are committed to making you and your sites successful.
We are committed to making you and your sites successful.
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.
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
“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 Site Enablement on a Global Scale
Florence now supports workflows between sponsors and more than 10,000 study sites in 45 countries.
