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Study ID: HUM00139068 IRB: IRB MED Date Approved: 6/7/2021 Expiration Date: 6/1/2022UNIVERSITY OF MICHIGAN AND HURLEY MEDICAL CENTER CONSENT TO BE PART OF A RESEARCH STUDY 1. KEY INFORMATION ABOUT
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To fill out IRB forms and submissions, follow these steps:
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Start by gathering all the necessary information and documents required for the IRB form.
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Begin filling out the form, paying attention to all the required fields and providing accurate information.
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If you are unsure about any particular section or question, consult with the IRB office or a supervisor for clarification.
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Gather any supporting documents or appendices that need to be submitted along with the form.
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Submit the form and the required documents to the appropriate IRB office or designated personnel for review.
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Follow up with the IRB office regarding the status of your submission and address any additional requests or feedback provided by the IRB.
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IRB forms and submissions are typically required by individuals or organizations conducting research involving human participants.
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This includes researchers in fields such as psychology, medical sciences, social sciences, and others.
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Universities, research institutions, and other organizations involved in research activities also need to complete IRB forms and submissions.
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Compliance with IRB requirements ensures that ethical considerations and participant safety are upheld during research studies.
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IRB forms and submissions refer to the documents required by Institutional Review Boards (IRBs) for the review and approval of research involving human participants, ensuring ethical standards are maintained.
Researchers and institutions conducting studies involving human subjects are required to file IRB forms and submissions before initiating their research.
To fill out IRB forms and submissions, researchers must provide detailed information about the study's purpose, methodology, participant recruitment, informed consent, and data management, adhering to specific guidelines set by the reviewing IRB.
The purpose of IRB forms and submissions is to ensure the ethical treatment of participants, minimize risks, and safeguard the rights and welfare of individuals involved in research.
Information reported on IRB forms must include study title, research objectives, methodology, potential risks and benefits, informed consent procedures, and participant demographics.
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