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APPLICATION FORM INITIAL REVIEW INSTITUTIONAL REVIEW BOARD/HUMAN SUBJECTS COMMITTEE Office of Sponsored Programs 5500 N. St. Louis Ave. , Building C Third Floor Phone: 773/4424672 / Fax:773/4424673www.neiu.edu/sprogram
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How to fill out institutional review boardhuman subjects

01
To fill out the institutional review board human subjects, follow these steps:
02
Review the guidelines and regulations provided by your institution or organization regarding human subjects research and the Institutional Review Board (IRB) process.
03
Obtain the necessary forms and documents from the IRB office or the designated committee.
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Fill out the required information on the forms, including details about the research project, purpose, methodology, and the potential risks and benefits for human subjects.
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Ensure all necessary signatures are obtained, including those of the principal investigator, co-investigators, and any other relevant personnel involved in the research.
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Provide any supporting documents, such as informed consent forms, recruitment materials, questionnaires, or surveys that will be used in the research study.
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Submit the completed forms and documents to the IRB office within the specified deadline.
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Await review and approval from the IRB committee. They may request revisions or clarifications before granting approval.
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Once approved, adhere to the IRB guidelines throughout the research process and ensure ongoing compliance with any reporting or monitoring requirements.
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Maintain proper documentation of all interactions with human subjects, including informed consent forms and any modifications to the research protocol.
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Report any adverse events or non-compliance issues to the IRB as required.
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It is advisable to consult with your institution's IRB office or seek guidance from experts to ensure compliance with ethical and legal obligations during the process.

Who needs institutional review boardhuman subjects?

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Various individuals and entities may need to go through the Institutional Review Board (IRB) process for human subjects research.
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Academic researchers: Researchers conducting studies at academic institutions, including universities and colleges, often need to obtain IRB approval.
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Medical professionals: Doctors, nurses, and other healthcare professionals conducting research involving human subjects may require IRB approval.
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Pharmaceutical companies: Companies involved in clinical trials or research on pharmaceutical products that involve human subjects typically need IRB approval.
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Government agencies: Government departments or agencies conducting research with human subjects may need to comply with IRB protocols.
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Non-profit organizations: Non-profit organizations engaging in research that involves human subjects may be required to seek IRB approval.
07
Independent researchers: Any individual conducting research that involves human subjects and intends to publish or present the findings may benefit from going through the IRB process.
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The exact requirements for IRB approval may vary depending on the institution, the nature of the research, and applicable laws and regulations.

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The Institutional Review Board (IRB) is a committee that is responsible for reviewing and approving research studies involving human subjects to ensure their rights and welfare are protected.
Researchers and institutions conducting research studies involving human subjects are required to file with the Institutional Review Board (IRB).
To fill out the IRB application, researchers must provide detailed information about their study protocol, potential risks and benefits to participants, informed consent process, and procedures for protecting confidentiality.
The purpose of the Institutional Review Board (IRB) is to protect the rights and welfare of human subjects participating in research studies, by ensuring that the study meets ethical standards and regulatory requirements.
Researchers must report detailed information about study protocol, potential risks and benefits to participants, informed consent process, procedures for protecting confidentiality, and any conflicts of interest.
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