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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.
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/.
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AT A GLA NCE
Florence eBinders™ is a secure, FDA Part 11 and HIPAA-compliant system that replaces paper forms and physical binders, giving research teams an efficient, compliant way to electronically sign, manage, store, and collaborate on study documents and to facilitate remote monitoring.
Eligibility
Faculty, Professional Staff
Rates
Not applicable.
Getting Started
https://drexel.edu/medicine/research/clinical-trials/florence-ebinders/
Requesting Help
HELP DOCUMENTATION
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