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Morehouse School of Medicine INSTITUTIONAL REVIEW BOARD GUIDELINES, POLICIES & PROCEDURES FOR THE PROTECTION OF HUMAN SUBJECTS Institutional Review Board Morehouse School of Medicine 720 West view
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How to fill out institutional review board

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How to fill out institutional review board:

01
Identify the form: Begin by obtaining the specific form required for the institutional review board (IRB) application. This form can typically be found on the IRB's website or by contacting the IRB office directly.
02
Gather necessary information: Before filling out the form, gather all the required information and documents. This may include the research proposal, informed consent forms, supporting documents, and any other relevant materials.
03
Follow instructions: Carefully read through the instructions provided on the form. Make sure to understand the requirements, guidelines, and any specific regulations or protocols that need to be followed.
04
Provide project details: Start filling out the form by providing the necessary project details, such as the title, principal investigator's name, research team members, and the project's funding source.
05
Explain the research: Describe the purpose, objectives, and background of the research project. Provide a clear and concise summary of the research methodology, including the study design, recruitment process, data collection methods, and analysis techniques.
06
Address ethical considerations: In a separate section, elaborate on the ethical considerations of the research. Explain how participant confidentiality and privacy will be protected, any potential risks involved, and how informed consent will be obtained from participants.
07
Submit supporting documents: Attach any required supporting documents, such as informed consent forms, questionnaires, recruitment materials, and any other necessary paperwork.
08
Review and revise: After completing the form, carefully review all the information provided. Make sure it is accurate, logical, and meets the requirements outlined by the IRB. Correct any errors and make necessary revisions.
09
Obtain necessary approvals: Once the form is completed and reviewed, submit it to the IRB office. The IRB will evaluate the application, review the research proposal, and assess its ethical considerations. If any revisions are required, make the necessary changes and resubmit the form.

Who needs an institutional review board?

01
Academic researchers: University-affiliated researchers, including professors, students, and research staff, often require IRB approval for their studies involving human participants.
02
Medical professionals: Those involved in medical research, such as doctors, nurses, and researchers in healthcare institutions, are typically required to submit their research projects to the IRB.
03
Pharmaceutical companies: Pharmaceutical corporations conducting clinical trials or research involving human subjects need to seek IRB approval to ensure ethical considerations.
04
Non-profit organizations: Non-profit organizations conducting research studies that involve human participants are also required to go through the IRB process to ensure the protection and welfare of the participants.
05
Government agencies: Government-funded research projects involving human subjects usually require IRB approval to ensure compliance with ethical guidelines and regulations.
06
Private institutions: Private research institutions, independent researchers, and any other individuals or entities conducting studies involving human participants may need to obtain IRB approval depending on the nature and scope of their research.
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The institutional review board is a committee that is responsible for reviewing and approving research studies involving human subjects.
Researchers conducting studies involving human subjects are required to file with the institutional review board.
Researchers must submit the necessary forms and documentation as required by the institutional review board.
The purpose of the institutional review board is to protect the rights and welfare of human subjects participating in research studies.
Researchers must report details about their study design, methods, risks, benefits, and informed consent procedures.
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