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AUBURN UNIVERSITY INSTITUTIONAL REVIEW BOARD for RESEARCH INVOLVING HUMAN SUBJECTS R E S E A R C H P R O T O C O L R E V I E W F O R M For Information or help contact THE OFFICE OF RESEARCH COMPLIANCE,

How to fill out irb protocol review form

How to fill out an IRB protocol review form:

1. Begin by carefully reading the instructions provided on the form or any accompanying documents. This will give you an overview of the information required and the specific guidelines for completing the form.
2. Start by providing basic information about the research project, such as the title, principal investigator's name, and contact details. Include any collaborating institutions or individuals involved in the study.
3. Clearly state the objective of the research and provide a detailed description of the study design, methodology, and procedures. This section should include information about the participant population, recruitment methods, and informed consent process.
4. Describe any potential risks or discomforts that participants may experience during the study. It is important to thoroughly analyze and document any risks and provide plans for mitigating or minimizing them. This demonstrates your commitment to safeguarding the welfare of participants.
5. Outline the benefits of the research, both to the participants and to society as a whole. Explain how the potential benefits outweigh any potential risks or discomforts.
6. Describe the process of obtaining informed consent from participants, ensuring they have a clear understanding of the research objectives, procedures, risks, benefits, and their rights as participants. Include a copy of the informed consent form with the protocol review form.
7. Explain how the data collected will be handled, stored, and protected to ensure participant confidentiality. Discuss any data management or security measures in place to protect participant privacy.
8. Indicate any external resources, such as funding sources or collaborations, that are associated with the research project.
9. If applicable, provide a plan for monitoring the progress of the research, including any auditing or data validation procedures.
10. Submit the completed IRB protocol review form along with any supporting documents, such as consent forms, recruitment materials, and study protocols, to the appropriate regulatory body for review.

Who needs an IRB protocol review form?

Researchers and institutions conducting human subjects research are typically required to complete an IRB protocol review form. This includes researchers in fields such as medicine, psychology, sociology, anthropology, and other social and behavioral sciences. The purpose of the IRB review is to ensure that the research project is ethical, protects the rights and welfare of participants, and follows applicable regulations and guidelines. IRB protocol review forms are necessary to seek approval from the Institutional Review Board (IRB) or other ethics committees before conducting research involving human subjects.

For pdfFiller’s FAQs

What is irb protocol review form?

The IRB protocol review form is a document used to submit research proposals to the Institutional Review Board (IRB) for review and approval.

Who is required to file irb protocol review form?

Researchers conducting studies involving human subjects are required to file the IRB protocol review form.

How to fill out irb protocol review form?

To fill out the IRB protocol review form, researchers need to provide information about their study design, objectives, methodology, potential risks and benefits, informed consent process, and measures taken to ensure participant confidentiality.

What is the purpose of irb protocol review form?

The purpose of the IRB protocol review form is to ensure that research involving human subjects is ethically conducted, with adequate protections for participant safety and welfare.

What information must be reported on irb protocol review form?

The IRB protocol review form requires researchers to report detailed information about their research study, including the study design, participant recruitment procedures, data collection methods, potential risks and benefits, and plans for data analysis and dissemination.

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