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This document outlines the categories of research activities involving human subjects that may be exempt from full committee review, detailing the requirements and procedures for obtaining informed
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How to fill out exempt protocol summary form

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How to fill out Exempt Protocol Summary Form

01
Begin by downloading the Exempt Protocol Summary Form from the relevant institution's website.
02
Fill in the title of the project at the top of the form.
03
Provide a brief description of the research purpose and objectives.
04
List the researchers involved in the project, including their roles.
05
Indicate the methods of data collection and analysis you plan to use.
06
Specify the target population and how participants will be recruited.
07
Describe any potential risks to participants and how you plan to mitigate them.
08
Confirm that ethical standards will be maintained throughout the research.
09
Review all completed sections for accuracy and completeness.
10
Submit the form as instructed by your institution's guidelines.

Who needs Exempt Protocol Summary Form?

01
Researchers conducting studies that are considered exempt from full IRB review.
02
University faculty and students who are planning low-risk research projects.
03
Individuals affiliated with institutions that require documentation of exempt status for research.
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The Exempt Protocol Summary Form is a document used to summarize research protocols that are exempt from full review by an Institutional Review Board (IRB).
Researchers or institutions conducting studies that qualify for exemption under specific regulatory criteria are required to file the Exempt Protocol Summary Form.
To fill out the Exempt Protocol Summary Form, provide details such as the research title, description of the study, the rationale for exemption, participant information, and data collection methods, adhering to the formatting requirements outlined by the IRB.
The purpose of the Exempt Protocol Summary Form is to ensure that research projects claiming exemption are documented and that ethical considerations are assessed, even if they do not require full IRB review.
Information that must be reported includes study title, research objectives, participation criteria, informed consent procedures, data management plans, and the specific exemption category under which the study qualifies.
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