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Initial Version Date: 05/23/13 (IRB Approved: August 1, 2013) Amendment 1.0, dated 11.14.2013 PROTOCOL: PROSPECTIVE AND RANDOMIZED STUDY OF FIXED VERSUS FLEXIBLE PROPHYLACTIC ADMINISTRATION OF GRANULOCYTE
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Start by gathering all necessary information and documentation related to your research project.
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Researchers and research institutions conducting studies involving human subjects typically need to fill out IRB templates for review and approval by the institutional review board.
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The Institutional Review Board (IRB) is a committee established to review and approve research involving human subjects to ensure that ethical standards are met.
Researchers and institutions conducting studies involving human subjects are required to file with the IRB.
To fill out the IRB application, applicants must provide information about the study's purpose, methodology, participant recruitment, informed consent process, and potential risks and benefits.
The purpose of the IRB is to protect the rights and welfare of human research participants by ensuring all research complies with ethical standards.
Information required includes study title, principal investigator details, study aims, research design, participant selection criteria, informed consent process, and risk assessments.
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