Eliminate Paper Binders And Accelerate Clinical Trial Workflows With Florence eBinders

Clinical research sites are under constant pressure to start studies faster, stay inspection-ready, and manage growing document workloads. Paper binders and disconnected systems slow teams down, increase risk, and make it harder to scale research operations.

Florence eBinders digitizes your Investigator Site File and study workflows so research teams can manage regulatory documents, study logs, and participant binders in one secure platform. Instead of chasing signatures, managing spreadsheets, and preparing for monitor visits, your team can automate document workflows, enable remote collaboration, and maintain always-on compliance.

Run Studies Faster with Florence eBinders

Digitize your investigator site file

Manage regulatory documents, study logs, and participant binders in a single digital workspace.

Accelerate study startup

Automate document collection, approvals, and signatures to reduce delays and activate studies faster.

Enable secure remote monitoring

Provide sponsors and monitors with compliant access to source documents and study records without on-site visits.

Maintain inspection readiness

Automated audit trails, version control, and permission management help ensure compliance at every stage of the trial.

Manage multiple studies and locations

Collaborate across teams, studies, and locations with centralized document management and shared workflows.

Gain real-time operational visibility

Track missing documents, upcoming expirations, and outstanding tasks with study dashboards and alerts.

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