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A. Under the Revised Common Rule, the regulations no longer require annual continuing review for minimal risk (expedited) research studies. The IRB may; 1) still require a continuing review, 2) require submission of a progress report at periodic intervals, or 3) not require additional reporting on the studys progress.
Continuing Review is the process by which the IRB re-evaluates whether a protocol is being conducted in compliance with the criteria for approval that are applied during initial review.
Studies meeting expedited review criteria and studies that have met a certain status (e.g. in data analysis) do not require a full continuation review, however the study team remains responsible for providing the IRB with an update on the study on an annual basis.
Institutional Review Board (IRB) The primary purpose of the IRB is to protect the rights and welfare of human subjects involved in research activities being conducted under its authority.
This group review serves an important role in the protection of the rights and welfare of human research subjects. The purpose of IRB review is to assure, both in advance and by periodic review, that appropriate steps are taken to protect the rights and welfare of humans participating as subjects in the research.
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There are three major types of review: Exempt, Expedited, and Full.

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