OVERVIEW OF SERVICE
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.
DESCRIPTION & FEATURES
- 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.
Eligibility
Faculty, Professional Staff
Rates
Not applicable.
GETTING STARTED
Information about investigator, monitor, and coordinator training available at https://drexel.edu/medicine/research/clinical-trials/florence-ebinders/.
REQUESTING HELP
Janet Matthews, MSN, RN, Senior Director for Research Program Development at jm834@drexel.edu.
ADDITIONAL INFORMATION
More information is available at https://drexel.edu/medicine/research/clinical-trials/florence-ebinders/.