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Irene Instructions for Central Michigan University www.irbnet.org XII. Consent/permission/assent formal consent documents should be created using the templates in the Form Library. Notice that there
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Read through the form to understand the requirements and instructions.
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Fill in the required information such as participant details, study purpose, and risks involved.
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Researchers and organizations conducting studies involving human participants
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Institutional Review Boards (IRBs) responsible for reviewing and approving research protocols
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Participants who are being asked to provide informed consent or assent to participate in a study
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IRBNet consent and assent forms are documents used to obtain informed consent from participants involved in research studies, ensuring they understand the study's purpose, procedures, risks, and benefits.
Researchers conducting studies that involve human subjects are required to file IRBNet consent and assent forms.
To fill out the IRBNet consent and assent forms, researchers should provide clear and comprehensive information about the study, including its aims, procedures, risks, benefits, and participant rights, and ensure participants understand this information.
The purpose of IRBNet consent and assent forms is to ensure ethical standards in research by obtaining informed consent from participants, thus protecting their rights and welfare.
The forms must report information such as the study title, study purpose, procedures, potential risks, benefits, confidentiality, and participants' rights.
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