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Questions regarding IRRB submissions can be directed to 330 344-6947 or by emailing IRRB akrongeneral.org. Cleveland Clinic Akron General FOR IRRB USE ONLY IRRB Number IRRB Reviewer Exempt Expedited Full Institutional Research Review Board Akron General Medical Center Notification of Closure of Human Subjects Research Study Please type all of the required information. HAND WRITTEN FORMS WILL NOT BE ACCEPTED. Submit an electronic copy of the completed and signed form to the Institutional...
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How to fill out institutional research review board

01
Step 1: Obtain the necessary application form for the Institutional Research Review Board (IRRB).
02
Step 2: Familiarize yourself with the research protocols and guidelines set forth by the IRRB.
03
Step 3: Complete the application form, providing detailed information about your research project.
04
Step 4: Submit the application form along with any required supporting documents to the IRRB office.
05
Step 5: Await review and approval from the IRRB.
06
Step 6: If necessary, make any suggested revisions or modifications to your research project.
07
Step 7: Once approved, commence your research while adhering to the guidelines and protocols outlined by the IRRB.
08
Step 8: Periodically update the IRRB on the progress and any changes in your research project.
09
Step 9: Upon completion of your research, provide a final report to the IRRB.
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Step 10: Ensure all ethical considerations and regulatory requirements related to your research are met.

Who needs institutional research review board?

01
Researchers conducting studies involving human subjects.
02
Institutions involved in research activities, such as universities, hospitals, and research organizations.
03
Individuals or organizations receiving funding for research projects.
04
Researchers working in fields where ethical considerations are paramount, such as medical, psychological, or social sciences.
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The institutional research review board is a committee that reviews and approves research projects involving human subjects to ensure ethical standards and compliance with regulations.
Researchers conducting studies involving human subjects are required to file with the institutional research review board.
To fill out the institutional research review board, researchers must provide detailed information about their study protocols, potential risks to participants, and methods for obtaining informed consent.
The purpose of the institutional research review board is to protect the rights and well-being of human subjects participating in research studies.
Researchers must report detailed study protocols, informed consent procedures, potential risks to participants, and methods for protecting confidentiality of data.
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