Summary: Presented By
Amanda A. Hastings, DRIC Education Specialist
Joanna Haller, Human Research Protection Program Manager
 What is the IRB?
Human Subject Research Defined
What IS Informed Consent?
PI-Initiated Studies & PI Responsibility
Submitting a Study
What to Expect during Review
Timeframes and Timetables
Post-Approval ­ Now What?
Question and Answer
 IRB is an acronym for Institutional Review
Board
The IRB is responsible for the review and
approval of all research involving human
subjects
Scientific validity
Ethical review
Per Federal regulations (45CFR46) IRBs are

Source: Arslan, Hüseyin - Department of Electrical Engineering, University of South Florida

Collections: Engineering