Florence eBinders provides automated compliance, remote monitoring and site wide visibility with global dashboards to help us tackle study tasks more efficiently and accelerate study start-up. Florence eBinders advances clinical research through Part 11-compliant purpose-built software. This is a validated 21 CFR Part 11 and HIPAA compliant service that manages both regulatory and source documents.

• Store and manage study documents.
• Collaboration.
• Remote monitoring.
• Electronic signatures.
• Integrates with other tools and systems such as CTMS, IRB Portals, EDC et.
• Generates reports on document status, user activity and other relevant metrics for analytic analysis.
• Supports access and functionality via mobile devices, ensuring flexibility and convenience for users.
• Ensures security and compliance via a validated 21 CFR Part 11 and HIPAA compliant service.

See information on getting started here: https://drexel.edu/medicine/research/clinical-trials/florence-ebinders/

Information about investigator, monitor, and coordinator training available at https://drexel.edu/medicine/research/clinical-trials/florence-ebinders/.

Janet Matthews, MSN, RN, Senior Director for Research Program Development at jm834@drexel.edu.

More information is available at https://drexel.edu/medicine/research/clinical-trials/florence-ebinders/.