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Quick Start Guide and Frequently Asked Questions (FAQs) To be used with the guidance document: Determining Which Activities Require Greenville Health System (GHS) Human Research Protection Program (HRPP)/Institutional Review Board (IRB) Review. Will the research activity involve collecting:
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Quick Start Guide and Frequently Asked Questions (FAQs)To be used with the guidance document: Determining Which Activities Require Greenville Health System (GHS) Human Research Protection Program (HRPP)/Institutional Review Board (IRB) Review Will the research activity involve collecting: Information about living individuals through intervention, interaction or observation? OR Identifiable private information about individuals? No IRB submission required NO YES What is the purpose of the study? Quality Improvement Project Research QI for Internal GHS only Quality Improvement project wiith intent to publish or present outside GHS What is the risk to human subjects? No more than minimal risk (chart reviews; observational studies) More than minimal risk (clinical Investigation with research subjects contact? (e.g. clinical trials, patient interviews, etc.)) No IRB submission required Submit Expedited IRB application Submit Full-Board application Version 18JUN2014