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NEW JERSEY CITY UNIVERSITY INSTITUTIONAL REVIEW BOARD Procedures and Guidelines for Researchers for the Protection of Human Participants Upon completion of IRB Application, please submit to The Office
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How to fill out institutional review board

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How to Fill out an Institutional Review Board (IRB):

01
Start by conducting thorough research on the specific requirements and guidelines set forth by the IRB. Familiarize yourself with the forms, documents, and protocols that need to be completed.
02
Begin by completing the necessary administrative paperwork, which usually includes providing information about the research project, the principal investigator, and any other personnel involved.
03
Ensure that you have obtained informed consent forms, if applicable, for the participants in your study. These forms should clearly outline the nature of the research and provide a space for participants to indicate their willingness to participate.
04
Compile all relevant supporting documents, such as research protocols, survey questionnaires, interview guides, or any other materials that will be used during the research process. Ensure that these documents align with the ethical standards established by the IRB.
05
Double-check that all necessary signatures and dates are included on the required forms. This may include the signature of the principal investigator, co-investigators, participants, or any other relevant parties.
06
Review and revise your submission to ensure that it is complete, accurate, and aligns with the IRB's expectations. Pay attention to any specific formatting or organization requirements outlined by the IRB.
07
Submit your filled-out IRB application and accompanying materials according to the specified submission process. This may involve electronic submission, mailing, or hand-delivery, depending on the IRB's preferences.

Who Needs an Institutional Review Board (IRB)?

01
Researchers conducting studies involving human participants typically need to obtain IRB approval. This can include academic researchers, medical professionals, social scientists, or individuals working in industry.
02
Institutions such as universities, hospitals, nonprofit organizations, or any other entity conducting research involving human subjects are required to have an IRB in place. This ensures the ethical treatment and protection of participants involved in the research process.
03
Funding agencies and regulatory bodies often require researchers to undergo the IRB review before approving research grants or permits. This helps to ensure that the proposed research is conducted safely, ethically, and with proper oversight.
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An institutional review board (IRB) is a committee that is responsible for reviewing and approving research involving human subjects to ensure their safety and ethical treatment.
Researchers, institutions, and organizations conducting research involving human subjects are required to file an institutional review board.
To fill out an institutional review board, researchers must submit an application that includes details about the research protocol, risks to participants, and consent forms.
The purpose of the institutional review board is to protect the rights and welfare of human subjects participating in research studies.
The institutional review board requires information on the research protocol, risks and benefits to participants, informed consent process, and any potential conflicts of interest.
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