This page provides information about the different types of review that your protocol can undergo. If you are unsure whether your project qualifies as “research involving human subjects”, please visit the Does Your Project Require IRB Review page.
In order for research to qualify as exempt, the project must fall into at least 1 of 8 federally-defined exempt categories and present no risk or no greater than minimal risk to the participants. Although this category is called exempt, this type of research does require prospective IRB review. Researchers must submit an exempt application in order for the HSC to assess whether the project qualifies as exempt research. Projects that are low risk may be considered exempt. Some examples of exempt research are:
Exempt Limited Review
In certain exempt categories, collection of identifiable information, even if considered sensitive, may be eligible for exemption if the HSC has determined there are adequate provisions to protect the privacy of subjects and to maintain confidentiality of the data. In these instances the HSC will consider:
In order for research to be eligible for expedited review, the activities must be considered no greater than minimal risk to the human subjects and fall into at least 1 of 9 federally-defined categories. Once a project is submitted for review, the HSC will assess the level of risk to the human subjects. Some examples of expedited research are:
Full Board Review
Studies that might be considered greater than minimal risk and do not qualify for exempt or expedited review are reviewed at a convened meeting of the HSC by full board review. The HSC will conduct a risk assessment of studies that are reviewed by full board. Some examples of research reviewed by full board are:
Please see the submission deadlines page for Exempt, Expedited and Full Board review dates.