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This document serves as an application for researchers to request exemption from full Institutional Review Board (IRB) review for certain categories of research that qualify under federal regulations.
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How to fill out application for exemption from

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How to fill out APPLICATION FOR EXEMPTION FROM FULL IRB REVIEW

01
Obtain the APPLICATION FOR EXEMPTION FROM FULL IRB REVIEW form from your institution's IRB office or website.
02
Fill in the title of your research project at the top of the form.
03
Provide your name, contact information, and any relevant affiliations.
04
Describe the purpose of your research in clear and concise terms.
05
Identify the specific population or group that will be involved in your study.
06
Outline the methodology you will use for conducting your research.
07
Explain how you will collect data and ensure the confidentiality of participants.
08
Provide justification for seeking exemption from full IRB review based on the provided criteria.
09
Review the completed application for accuracy and completeness.
10
Submit the application to your institution’s IRB for consideration.

Who needs APPLICATION FOR EXEMPTION FROM FULL IRB REVIEW?

01
Researchers or individuals planning a study that involves minimal risk and fits the criteria for exemption as outlined by the IRB.
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“Exempt” research are human subjects studies that present no greater than minimal risk to subjects and fit into one or more exempt categories. Research that qualifies for an exempt determination do not have the same federal requirements for research found in expedited or full board review.
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.
Human subjects' research not falling into one of these categories requires convened board review. Exempt and expedited reviews are delegated reviews, which are screened by IRB staff and undergo final review by 1-2 IRB members.
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.
Examples of Commonly Exempted Research The following types of research are commonly processed under exempt review: Research on educational practices or educational curriculums. Benign behavioral interventions with adult subjects. Anonymous surveys or interviews on non-sensitive topics.
Research can qualify for an exemption if it is no more than minimal risk and all of the research procedures fit within one or more of the exemption categories in the federal IRB regulations. Studies that qualify for exemption must be submitted to the IRB for review before starting the research.
“Exempt” 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.
Examples of Commonly Exempted Research Research on educational practices or educational curriculums. Benign behavioral interventions with adult subjects. Anonymous surveys or interviews on non-sensitive topics. Passive observation of public behavior without collection of identifiers.

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It is a request submitted to the Institutional Review Board (IRB) seeking exemption from the full review process for research involving human subjects.
Researchers conducting studies that may qualify for exemption due to minimal risk or specific categories outlined by the IRB are required to file this application.
Researchers should complete the application form by providing required details about the study, including its purpose, design, participant eligibility, and how it meets exemption criteria.
The purpose is to expedite the review process for studies that pose minimal risk to participants while ensuring compliance with ethical standards.
Key information includes study title, principal investigator details, description of research activities, data collection methods, participant recruitment plans, and justification for exemption.
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