Exempt Survey
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How to fill out Exempt Survey?
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FAQ
Some examples of Exempt research are: anonymous or identifiable surveys or interviews. passive observation of public behavior with or without the collection of identifiers. retrospective and prospective medical chart reviews (allowable under specific criteria for UCI Healthcare Workforce)
Exempt research are human subjects studies that present no greater than minimal risk to subjects and fit into one or more exempt categories (as described below).
Exempt studies involve human subjects research: research involving a living individual about whom data. or biospecimens are obtained/used/studied/analyzed through interaction/intervention, or identifiable, private information is used/studied/analyzed/generated.
To be classified as exempt, the research:Cannot involve any of the exceptions for the exempt categories for research that involves children ; For studies subject to pre-2018 Common Rule requirements: The study cannot involve prisoners as research subjects. Cannot be greater than minimal risk.
Non-Exempt Research (Needs IRB Approval): Any research, inclusive of surveys that involves minors, prisoners, clinical populations; inclusive of any clients in any therapeutic setting/relationship with a potential researcher; and any other vulnerable populations, such as older adults, should undergo IRB review.
Research can be approved as exempt if it is no more than minimal risk and fits one of the exempt review categories as defined by federal regulation 45 CFR 46. Studies that may qualify for Exempt must be submitted to the IRB for review. Exempt reviews are conducted by a member of IRB staff.
In order to establish an individual research project as exempt, an investigator must complete an IRB application. On the IRB application the investigator should indicate the number of the category under which an exemption is claimed. Final determination as to whether a project is exempt rests with the IRB.
No full board review: An exempt protocol does not need full board review; modifications do not need to be reviewed at a full board meeting unless the protocol modifications change the exemption status.