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0Institutional Review Board
Human Subjects Protection
Training
May 8, 2024,
Paul Cam arena, MPH
IRB Analyst
Cynthia Robles, MPH
IRB ResidentVersion: Updated October 10, 2023Training Objectives
After
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How to fill out institutional review board

How to fill out institutional review board
01
Understand the purpose and guidelines of the IRB.
02
Obtain all necessary documentation and forms for the research study.
03
Submit the research study proposal to the IRB for review.
04
Prepare to address any concerns or questions raised by the IRB during the review process.
05
Receive approval from the IRB before initiating the research study.
Who needs institutional review board?
01
Researchers conducting studies involving human subjects.
02
Institutions or organizations receiving federal funding for research projects.
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What is institutional review board?
An institutional review board (IRB) is a committee that reviews and approves research involving human subjects, ensuring that ethical standards are met and that the rights and welfare of participants are protected.
Who is required to file institutional review board?
Researchers conducting studies involving human subjects, including faculty, staff, and students, are required to file with the institutional review board.
How to fill out institutional review board?
To fill out an institutional review board application, researchers should gather project details, including study protocol, informed consent forms, recruitment methods, and potential risks. They then complete the IRB application form provided by their institution, attaching all necessary documents.
What is the purpose of institutional review board?
The purpose of an institutional review board is to protect the rights, welfare, and well-being of human subjects involved in research, ensuring compliance with ethical standards and regulations.
What information must be reported on institutional review board?
Researchers must report the study's purpose, methodology, participant recruitment strategies, potential risks and benefits, informed consent processes, and any conflicts of interest.
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