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Aurora IRB Protocol for Research Involving Human Subjects Modification Form (IRB Chair or designee) Approval date: Expedited Full Category: 46.110(b)(2)/56.110(b)(2) conditions of approval were issued
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Protocol for research involving is a detailed plan of a scientific experiment or research study that includes information on the background, purpose, methodology, and ethical considerations.
Researchers, scientists, or any individual conducting research involving human subjects are required to file a protocol for review by an Institutional Review Board (IRB) or Ethics Committee.
The protocol for research involving can be filled out by providing detailed information on the study design, potential risks and benefits, recruitment methods, informed consent procedures, and data analysis plan.
The purpose of a protocol for research involving is to ensure that research studies are conducted ethically, with the well-being of participants as the top priority, and in compliance with regulatory requirements.
Information that must be reported on a protocol for research involving includes detailed study objectives, research methods, participant eligibility criteria, study procedures, and plans for data analysis and dissemination of results.
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