Single IRB (sIRB) Use and Administration
This course covers relying on a sIRB, serving as a sIRB of record, and authorization agreements.
The Single IRB (sIRB) Use and Administration course is intended for institutions relying on external IRBs and for sIRBs for multi-site research (including IRB administrators, researchers, and IRB members). It explores key considerations on external sIRB reliance, setting up and serving as a sIRB, and best practices for drafting, reviewing, and implementing authorization agreements between the sIRB and participating sites in multi-site research.
This course covers the National Institutes of Health (NIH) policy “Use of a Single Institutional Review Board for Multi-Site Research,” and the revised Common Rule (2018 Rule) cooperative research requirement.
Language Availability: English
Suggested Audiences: IRB Administrators, Researchers, Research Team Members, Institutional Review Boards (IRBs), Institutional/Signatory Officials, IRB Chairs, IRB Administrators and Staff, Human Subject Protection Staff, Students
Organizational Subscription Price: Included in a base subscription
Independent Learner Price: $29 per person
Explores key considerations when implementing sIRB relationships and what a participating site needs to do in preparation for relying on an external sIRB.
Recommended Use: Elective
ID (Language): 17387 (English)
Author(s): James Riddle, MCSE, CIP, CPIA - Advarra; Raffaella Hart, MSHS, CIP - BRANY IRB
Discusses key elements and considerations for setting up an IRB to serve as a sIRB.
Recommended Use: Elective
ID (Language): 17388 (English)
Author(s): James Riddle, MCSE, CIP, CPIA - Advarra; Raffaella Hart, MSHS, CIP - BRANY IRB
Introduces best practices for drafting, reviewing, and implementing authorization agreements between the sIRB and participating sites in multi-site research.
Recommended Use: Elective
ID (Language): 17392 (English)
Author(s): Cindy Gates, JD, RN, CIP - University of Miami