What are the five criteria an IRB must consider when approving research involving human subjects?
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A
Budget, timeline, sponsor reputation, site capacity, staff qualifications
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B
Risks minimized, risks reasonable to benefits, equitable subject selection, informed consent obtained, data safety monitored
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C
FDA approval, institutional approval, staff training, equipment validation, protocol review
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D
Regulatory compliance, financial viability, scientific merit, ethical oversight, publication plan