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\u201cExempt\u201d human subjects research is a sub-set of research involving human subjects that does not require comprehensive IRB review and approval because the only research activity involving the human subjects falls into one or more specific exemption categories as defined by the Common Rule.
Timely Review: The IRB and the staff aim to respond to the investigator within one week of receipt of the IRB submission. Depending upon the type of review (i.e., initial, amendment, continuation) expedited review approval may take from one to three weeks.
Exempt Research Although the category is called "exempt," this type of research does require IRB review and the determination of exemption must be made by the IRB. The exempt determination process is much less rigorous than an expedited or full-committee review.
The time to process an application depends on the complexity of the research study and the quality and completeness of the application submitted to the IRB. Other variables include whether the application can be approved by the IRB Chair or Chair Designee (expedited review) or by the full board.
The IRB office utilizes an initial pre-review screening process, during which an IRB analyst reviews each submission for completeness and compliance. The analyst may ask the PI to make changes to the submission before it is reviewed by the IRB (pre-review).

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The IRB office utilizes an initial pre-review screening process, during which an IRB analyst reviews each submission for completeness and compliance. The analyst may ask the PI to make changes to the submission before it is reviewed by the IRB (pre-review).
How long does IRB review take? An expedited or exempt review may take about two weeks. Studies requiring convened review may take three or more weeks.
Can the IRB approve a project "retroactively?" No. There is no provision in the federal regulations that allow for IRB approval of research that has already been conducted.
IRB must review all projects that meet the definition of research and that involve human subjects prior to any data collection to determine the appropriate level of review, and, as appropriate, approve them. There are three major types of review: Exempt, Expedited, and Full.
If the project does not include any interaction or intervention with human subjects or include any access to identifiable private information, then the project does not require IRB review.

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