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IRB #: STU00213826MOD0005 Approved by NU IRB for use on or after 1/19/2024 through 9/24/2024. Permission to Take Part in a Human Research Study Do not sign this consent if today's date is later than
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Start by inputting the name of the organization or individual requesting consent.
02
Include a brief description of the information being collected and the purpose for which it will be used.
03
Specify the methods by which consent will be obtained (e.g. signing a physical document or checking a box online).
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Include a section detailing the individual's rights regarding their personal information.
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Clearly state how the individual can withdraw their consent if desired.
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Provide contact information for questions or concerns about the consent document.

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Template consent document is a standardized form that outlines an individual's permission or agreement for a specific action or procedure.
Template consent document is typically required to be filed by individuals who are undergoing a medical procedure or participating in a research study.
Template consent document can be filled out by providing personal information, signing and dating the document, and acknowledging understanding of the content.
The purpose of template consent document is to ensure that individuals are fully informed about a specific action or procedure and voluntarily agree to participate.
Template consent document must include details about the procedure or study, potential risks, benefits, alternatives, and the individual's rights.
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