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Institutional Review Board (IRB) Section C: Informed Consent Researchers must obtain the informed consent of participants. In this section you will find the following topics: Elements of Informed
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The institutional review board (IRB) is a committee that is responsible for reviewing and approving research involving human subjects. Its primary purpose is to ensure the protection of the rights and welfare of the participants in the research study.
Researchers, institutions, and organizations that conduct research involving human subjects are typically required to file an institutional review board (IRB) application.
To fill out an institutional review board (IRB) application, researchers need to provide detailed information about their research protocol, including the purpose of the study, methodology, participant selection criteria, informed consent process, and plans for data collection and analysis. The application may also require supporting documentation such as a research proposal, consent forms, and any potential conflicts of interest.
The purpose of the institutional review board (IRB) is to ensure that research involving human subjects is conducted ethically and in accordance with applicable laws, regulations, and ethical guidelines. This includes protecting the rights and welfare of the research participants, minimizing risks, and promoting informed consent and voluntary participation.
The information that must be reported on an institutional review board (IRB) application typically includes details about the research study, such as the research objectives, study design, participant recruitment and selection methods, informed consent process, data collection procedures, potential risks and benefits, and plans for data confidentiality and storage.
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