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Rev 07/19/15 institutional Review Board (IRB) Checklist This checklist is intended to aid investigators in providing the documentation necessary to submit a research proposal involving human subjects
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How to fill out ohsu institutional review board

01
Obtain the necessary application forms from the OHSU Institutional Review Board (IRB) office.
02
Fill out the forms accurately and completely, providing all required information.
03
Include all relevant supporting documents, such as consent forms, study protocols, and recruitment materials.
04
Clearly explain the purpose of the research, the study methodology, and any potential risks or benefits to participants.
05
Ensure that all procedures and protocols comply with ethical guidelines and regulations.
06
Submit the completed application and supporting documents to the OHSU IRB office.
07
Wait for the IRB to review and approve the application before proceeding with the research.

Who needs ohsu institutional review board?

01
Researchers planning to conduct research involving human subjects at Oregon Health & Science University (OHSU) are required to obtain approval from the OHSU Institutional Review Board (IRB).
02
Students, faculty, and staff members involved in research projects that involve human subjects also need to go through the IRB process.
03
Any individual or organization conducting research at OHSU that involves the use of human subjects must seek IRB approval.
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The OHSU Institutional Review Board (IRB) is a committee that is responsible for reviewing, approving, and monitoring research involving human subjects to ensure the protection of their rights and welfare.
Researchers conducting studies involving human subjects are required to file with the OHSU Institutional Review Board.
Researchers can fill out the OHSU Institutional Review Board application online through the OHSU eIRB system.
The purpose of the OHSU Institutional Review Board is to ensure that research involving human subjects is conducted ethically and with proper consideration for the rights and welfare of the participants.
Researchers must report detailed information about their study protocol, risks and benefits to participants, informed consent process, and how participant data will be protected.
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