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MEMORANDUM TO INSTITUTIONAL REVIEW BOARDS / HUMAN SUBJECTS REVIEW COMMITTEE STO:Institutional Review Boards / Human Subjects Review CommitteesFROM: Narayana Pastry, Director, Displaced New Orleans
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01
Obtain a copy of the institutional review board (IRB) human subjects application form.
02
Fill out the application form completely, providing detailed information on the research study, the risks and benefits to participants, and the procedures that will be followed.
03
Provide necessary documentation, such as informed consent forms, recruitment materials, and data collection tools.
04
Submit the completed application form and all supporting documentation to the IRB for review.
05
Respond promptly to any requests for additional information or modifications to the research study.

Who needs institutional review boards human?

01
Researchers conducting studies involving human subjects.
02
Institutions and organizations that fund and oversee research involving human participants.
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Institutional Review Boards (IRBs) are committees that are responsible for reviewing and approving research studies involving human participants to ensure ethical standards are met.
Researchers conducting studies involving human participants are required to file with an IRB.
To fill out an IRB application, researchers must provide detailed information about their study protocol, the risks and benefits to participants, and how participant confidentiality will be protected.
The purpose of IRBs is to protect the rights and welfare of human research participants by ensuring that research studies meet ethical standards.
Information such as study protocols, participant risk assessments, and plans for informed consent must be reported to an IRB.
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