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Questions regarding IRRB submissions can be directed to 330 344-6497 or by emailing IRRB akrongeneral.org. Name of Institution B remains responsible for ensuring compliance with the IRB s determination and with the terms of its OHRP-approved FWA. Submit and electronic version of the completed form to the Institutional Research Review Board IRRB akrongeneral.org. This document must be kept on file by both parties and provided to OHRP upon request. Signature of Signatory Official Name of...
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How to fill out institutional research review board

01
Gather all necessary documents and information required for the institutional research review board application.
02
Review the guidelines and regulations provided by the institution for filling out the application.
03
Start by completing the basic information section of the application form, such as project title, principal investigator's name, and contact details.
04
Provide a detailed description of the research project, including its purpose, objectives, methodology, and expected outcomes.
05
Include information about the target population and any potential risks or benefits associated with the research.
06
Attach any supporting documents, such as informed consent forms, participant recruitment materials, or survey questionnaires.
07
Ensure all ethical considerations and measures for participant confidentiality are addressed in the application.
08
Proofread the entire application for any errors or omissions before submitting it to the institutional research review board.
09
Follow up with the board if any further information or revisions are required.
10
Once approved, adhere to the guidelines and regulations set forth by the institutional research review board throughout the research process.

Who needs institutional research review board?

01
Researchers conducting studies involving human subjects.
02
Academic institutions, universities, or research organizations that conduct research involving human subjects.
03
Funding agencies or sponsors that require ethical oversight of research projects.
04
Any research project that involves data collection, experimentation, or observation on human participants.
05
Projects that may have potential risks or benefits for the participants, such as medical, psychological, or social studies.
06
Projects that aim to contribute to scientific knowledge or address societal issues through research.
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The institutional research review board is a committee that reviews and approves research protocols to ensure the protection of human subjects.
Researchers conducting studies involving human subjects are required to file with the institutional research review board.
Researchers must fill out the required forms and submit them to the institutional research review board for review.
The purpose of the institutional research review board is to ensure the ethical and legal compliance of research studies involving human subjects.
Researchers must report details about the study protocol, informed consent process, and risks and benefits to participants.
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