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This document is an application for exempt research at the University of Sioux Falls. It outlines submission instructions, roles, required qualifications, and details about the study's purpose, participants,
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How to fill out exempt research application

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How to fill out Exempt Research Application

01
Begin by downloading the Exempt Research Application form from the appropriate website.
02
Fill out the title of your research project in the designated field.
03
Provide a brief description of the research objectives and methodology.
04
Identify the key participants and describe the criteria for their selection.
05
Outline any potential risks involved for participants and how you will mitigate them.
06
Include information on how data will be collected, stored, and protected.
07
Specify the duration of the research project and any funding sources.
08
Review all completed sections for accuracy and completeness before submission.

Who needs Exempt Research Application?

01
Researchers conducting studies that involve minimal risk to participants.
02
Academic institutions and organizations aiming to obtain approval for specific exemptions.
03
Any individual or group receiving funding for research that requires ethical review of exempt studies.
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Exempt Review Categories Include: Research conducted in established or commonly accepted educational settings, that specifically involves normal educational practices that are not likely to adversely impact students' opportunity to learn or the assessment of educators.
The common law research exemption is an affirmative defense to infringement where the alleged infringer is using a patented invention for research purposes. The doctrine originated in the 1813 decision by Justice Joseph Story appellate decision Whittemore v. Cutter, 29 Fed. Cas.
Human subjects research that is classified as “exempt” means that the research qualifies as no risk or minimal risk to subjects and is exempt from most of the requirements of the Federal Policy for the Protection of Human Subjects, but is still considered research requiring an IRB review for an exemption determination.
An “exempt” employee under California law may be paid on a salary basis, without overtime wages, without meal and rest periods, without certain record-keeping rights and without some of the other legal protections provided to workers who are nonexempt.
Human subjects research that is classified as “exempt” means that the research qualifies as no risk or minimal risk to subjects and is exempt from most of the requirements of the Federal Policy for the Protection of Human Subjects, but is still considered research requiring an IRB review for an exemption determination.
The common law research exemption is an affirmative defense to infringement where the alleged infringer is using a patented invention for research purposes. The doctrine originated in the 1813 decision by Justice Joseph Story appellate decision Whittemore v. Cutter, 29 Fed. Cas.
Expedited level of review Projects not eligible for an exempt review may be eligible for an expedited review. Expedited does not mean that the review is less rigorous or happens more quickly than convened review. It refers, instead, to certain types of research considered to involve minimal risk.

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An Exempt Research Application is a submission made to an Institutional Review Board (IRB) to determine whether a research study qualifies for exemption from full IRB review based on regulations that outline certain categories of research.
Researchers planning to conduct studies that may qualify as exempt according to federal regulations are required to file an Exempt Research Application with the IRB.
To fill out an Exempt Research Application, researchers must complete the designated form provided by the IRB, provide detailed information about the research project, including its purpose, methodology, and any potential risks to participants.
The purpose of the Exempt Research Application is to ensure that research involving human subjects is conducted ethically and in compliance with applicable regulations while allowing for certain low-risk studies to bypass the more extensive requirements of full IRB review.
Researchers must report information including the study's title, a description of the research, participant recruitment methods, potential risks and benefits, data management plans, and any funding sources.
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