Florence Workflows > Electronic Study Logs

Simplify Study Logs with Digital and Remote Workflows

Eliminate paper logs and complex systems from your workflows by creating, completing, reviewing and modifying any log in a globally compliant platform.

eDOA and eLogs Signature

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.

FDA Part 11 Compliance Logo
HIPAA Compliance Logo
ICH GCP Complaint Logo
GDPR Compliant Logo
EU Annex 11 Compliant Logo
EU-US Privacy Shield Compliant Logo

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.

Site Adoption Rate
Uptime Past 12 Months
Support Response Time

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.

Dr. Christina Brennan Headshot
Blue Quote Box

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.

Learn more about moving to Electronic Logs with Florence eBinders.