On Behalf of the Office of Clinical Trial Activation (OCTA), Clinical Trials Operations (CTO), and Academic Research Services (ARS), we’re pleased to announce the upcoming launch of Advarra’s eRegulatory Binder System.
UCSF’s Advarra eReg tool is a 21 CFR Part 11 compliant electronic regulatory binder, including participant source documents, designed to support efficient, compliant clinical research regulatory documentation.
Key Benefits:
- 21 CFR Part 11 Compliant
- Integration with UCSF’s OnCore Clinical Trial Management System
- Integration with Advarra CIRBI (for studies using this external IRB)
- Centrally managed solution at UCSF
Learn more by joining us for an overview of UCSF’s eReg at the upcoming CTO Forum on Wednesday, March 18th!