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Institutional Review Board GUIDELINE #5: RESEARCH INVOLVING SECONDARY USE OF DATA, DOCUMENTS, RECORDS OR SPECIMENSI. PURPOSE This guideline is to ensure that human subjects research conducted complies
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How to fill out human subjects research amp

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To fill out a human subjects research amp, follow these steps:
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Start by identifying the purpose of your research and the specific human subjects you will be studying.
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Determine if your research requires approval from an Institutional Review Board (IRB) or any other ethical review board.
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Begin by providing general information about your research, including the title, investigator's name, institution, and project description.
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Clearly define the inclusion and exclusion criteria for selecting human subjects.
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Describe the procedures and methods you will use for data collection, ensuring they are ethical and respectful of the subjects' rights.
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Address any potential risks or benefits associated with the research and how you plan to mitigate the risks and maximize the benefits.
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Include a section on informed consent, detailing how you will obtain consent from the participants and protect their confidentiality.
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Provide information about any incentives or compensation you plan to offer to the human subjects.
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Remember to always comply with the guidelines and regulations to ensure the ethical conduct of your research with human subjects.

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Human subjects research is research that involves collecting data from or about individuals, including their opinions, behaviors, or other personal information.
Researchers and institutions that conduct studies involving human subjects are required to file human subjects research applications.
To fill out the human subjects research application, researchers should provide detailed information about the study's purpose, methodology, participant recruitment, informed consent processes, and data confidentiality measures.
The purpose of human subjects research applications is to ensure that studies are conducted ethically, with respect for participant welfare and rights.
The application must report information such as study objectives, recruitment strategies, consent procedures, potential risks to participants, and data management plans.
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