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Institutional Review Board (IRB) FWA0000387320142015 Human Subjects Research ApplicationProtocol #: 1415Office Use Only. Investigator Information Principal Investigator*: Email: College/School: Department: Status:FacultyStaffDoctoral
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Step 1: Obtain the necessary documentation and forms for conducting human subjects research in 2014-2015.
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Step 2: Familiarize yourself with the ethical guidelines and regulations governing human subjects research.
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Step 3: Clearly define your research objectives and develop a research plan.
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Step 4: Identify potential human subjects for your research and obtain informed consent from them.
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Step 5: Collect and analyze the data according to your research plan.
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Step 6: Ensure the confidentiality and privacy of the human subjects' information.
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Step 7: Interpret the results of your research and draw conclusions.
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Step 8: Prepare a written report of your research findings.
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Step 9: Submit the report to the appropriate authorities or organizations as required.
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Step 10: Review and comply with any feedback or recommendations for future research.

Who needs 2014-2015 human subjects research?

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Researchers, scientists, or individuals conducting research involving human subjects in the years 2014-2015.
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Human subjects research application is a formal request submitted to an institution's Institutional Review Board (IRB) seeking approval to conduct research involving human participants.
Researchers who are planning to conduct studies involving human participants are required to file a human subjects research application.
To fill out a human subjects research application, researchers must provide detailed information about the study design, recruitment strategies, potential risks and benefits, and informed consent procedures.
The purpose of a human subjects research application is to ensure the protection of human participants in research studies by assessing the study's ethical considerations and compliance with regulations.
Information such as the study protocol, informed consent form, recruitment materials, data management plan, and potential risks and benefits must be reported on a human subjects research application.
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