![]() The following categories of research do not require continuing review: Research approved by Full Board review undergoes continuing review by the IRB at least once a year. Investigators should understand that while Expedited review is conducted by fewer individuals, it is no less stringent and not necessarily faster than a Full Board review. ![]() Protocols cannot be expedited if the research involves more than minimal risk. Non-exempt research undergoes either Expedited (subcommittee) review or Full Board review. Ensure that selection of subjects is equitableĪn IRB (Institutional Review Board) must review all human subjects research activities covered by the HHS regulations.Risk justified by benefits of the research.Ensure that risks to subjects are minimized.IRB assessment of risk/benefit analysis, including study design.threats of harm) or undue influence (e.g. Additional safeguards for protection of subjects likely to be vulnerable to coercion (e.g.Protecting privacy and maintaining confidentiality. ![]()
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