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University of Puget Sound INSTITUTIONAL REVIEW BOARD Application for Approval of Research Involving Human Subjects(Cover Sheet) (Protocols meeting Full Board Review must be submitted two weeks prior
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01
Start by logging into the online portal of the Institutional Review Board at the University of XYZ.
02
Navigate to the section for submitting a new application and click on 'Fill out application form'.
03
Enter your personal details such as name, email address, and contact information.
04
Provide information about the project for which you require the institutional review board approval.
05
Describe the purpose, methodology, and objectives of the project in detail.
06
Specify the target population for your research and any potential risks or benefits involved.
07
Upload any supporting documents such as consent forms, survey questionnaires, or study protocols.
08
Review the information provided and make sure all fields are accurately filled.
09
Once you are satisfied with the application, submit it for review by the Institutional Review Board.
10
Await the decision of the board and respond to any queries or requests for additional information if necessary.

Who needs institutional review boarduniversity of?

01
Researchers, faculty members, and students conducting research involving human subjects at the University of XYZ require the approval of the Institutional Review Board.

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An Institutional Review Board (IRB) is a committee established to review and approve research involving human participants to ensure that it is conducted ethically and in accordance with federal regulations.
Researchers, including faculty, students, and staff conducting studies involving human subjects are required to file with the Institutional Review Board.
To fill out an IRB application, researchers must provide details about their study, including the research protocol, informed consent document, data collection methods, and a description of how they will protect participants' rights and welfare.
The purpose of an Institutional Review Board is to protect the rights and welfare of human research subjects, ensure ethical standards are maintained, and to review research proposals for compliance with regulations.
Researchers must report information such as study objectives, methodology, participant recruitment strategies, informed consent processes, and how risks will be minimized.
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