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MSU USE ONLY IRB Log No.: MSU Proposal No: Institutional Review Board (IRB) Application for Amendment to a Previously Approved Protocol For Investigations Involving Human Participants Murray State
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How to fill out a institutional review board (IRB) application?

01
Start by gathering all the necessary information and documents required for the IRB application. This typically includes details about the research project, the purpose, methods, and potential risks or benefits involved.
02
Clearly define the target population or subjects involved in the research study. Explain why this specific group is chosen and provide relevant background information.
03
Outline the research procedures, methodology, and data collection techniques that will be used. Include details about any interventions or treatments that participants may receive, if applicable.
04
Describe the potential risks and benefits of participating in the research. Identify any foreseeable adverse events or discomfort that participants may encounter, and explain how these will be mitigated.
05
Develop a thorough informed consent form that will be provided to participants. This document should clearly explain the purpose, procedures, risks, benefits, and voluntary nature of participation. Ensure it is written in simple, understandable language and includes a space for participants to provide their signature indicating their informed consent.
06
Address the issue of participant confidentiality and privacy protection. Explain how data will be collected, stored, and analyzed while maintaining the anonymity and privacy of participants.
07
Provide details about the qualifications and credentials of the research team members who will be involved in the study. This helps establish their expertise and credibility in conducting the research ethically.
08
Include any appendices or supplemental materials required for the application, such as survey instruments, interview questions, or supporting literature.
09
Seek guidance or assistance from your institutional research office or IRB staff members throughout the application process. They can provide valuable feedback, answer questions, and ensure compliance with all regulations and guidelines.

Who needs an institutional review board (IRB)?

01
Researchers conducting studies involving human subjects are typically required to obtain IRB approval. This applies to a wide range of fields, including biomedical, social sciences, psychology, education, and more.
02
Institutions that receive funding from the federal government, such as universities, hospitals, and research organizations, usually have their own IRBs to oversee and review research conducted within their jurisdiction.
03
Participants or potential subjects in research studies also benefit from the existence of an IRB. The board's primary aim is to protect the rights, welfare, and well-being of human participants by ensuring that research is conducted ethically and in compliance with established regulations and guidelines.
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The Institutional Review Board (IRB) is a committee that is responsible for reviewing and approving research involving human subjects to ensure the protection of their rights and welfare.
Researchers and institutions conducting research involving human subjects are required to file an Institutional Review Board (IRB) application.
The IRB application typically requires detailed information about the research study, including the study design, risks and benefits to participants, informed consent procedures, and methods for ensuring participant confidentiality.
The purpose of the Institutional Review Board (IRB) is to protect the rights and welfare of human research subjects by ensuring that research is conducted ethically and in compliance with regulations.
The IRB application may require researchers to report details such as study protocols, recruitment materials, informed consent forms, data collection processes, and plans for data analysis and dissemination.
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