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! # Guidelines for Research on Human Subjects FACULTY/STUDENT RESEARCH HANDBOOK 2004-05 Table of Contents I. Introduction Page No. 1 Adherence to the Common Rule Official Definitions of Research and
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An institutional review board (IRB) is a committee responsible for reviewing, approving, and overseeing research studies involving human participants to ensure their rights, safety, and welfare are protected.
Researchers and institutions conducting research involving human participants are typically required to submit their study protocol to an institutional review board (IRB) for review and approval.
The process of filling out an institutional review board (IRB) application usually involves submitting a study protocol, consent forms, participant recruitment materials, and other relevant documents to the IRB. Each IRB may have its own submission process and requirements.
The purpose of an institutional review board (IRB) is to protect the rights, safety, and welfare of human participants involved in research studies. It ensures that the study protocols, consent procedures, and participant recruitment methods are ethically sound and comply with applicable regulations and guidelines.
The specific information required to be reported on an institutional review board (IRB) application may vary, but typically includes details about the study design, participant eligibility criteria, data collection procedures, potential risks and benefits, informed consent process, and confidentiality protections.
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