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Log Number (board use only)Indiana University of Pennsylvania Institutional Review Board for the Protection of Human SubjectsHuman Subjects Review ProtocolInvestigatorsPrincipal InvestigatorNameAcademic
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How to fill out institutional review board for

01
Start by gathering all the necessary documents and information, such as the research proposal, consent forms, and any relevant supporting materials.
02
Familiarize yourself with the specific guidelines and requirements of the institutional review board (IRB) you will be submitting to. These may vary depending on the institution or research field.
03
Fill out the necessary forms provided by the IRB. This may include the application form, consent form templates, and any additional forms required for your specific research study.
04
Provide a detailed description of your research study, including the purpose, methodology, participants, and any potential risks or benefits involved.
05
Ensure that all participant confidentiality and data protection measures are included in your application.
06
Obtain any necessary signatures from relevant parties, such as co-investigators, supervisors, or participants themselves.
07
Review and double-check all the information provided in the application forms to ensure accuracy and completeness.
08
Submit the completed application and supporting documents to the IRB according to their specified submission guidelines.
09
Wait for the IRB's review and approval or request for revisions. Be prepared to address any questions or concerns they may have.
10
Once approved, make sure to adhere to any conditions or guidelines set forth by the IRB throughout the duration of your research study.

Who needs institutional review board for?

01
Institutional review boards (IRBs) are typically required for any research involving human subjects. This includes both biomedical and social, behavioral, and educational research.
02
Researchers conducting clinical trials, experiments, surveys, interviews, or observations that involve human participants usually need to seek approval from an IRB.
03
Whether you are a student, academic researcher, scientist, or professional working in a research institution, you may need an IRB approval if your study involves human subjects.
04
IRBs are put in place to protect the rights, welfare, and safety of the research participants, ensuring that their consent is obtained, risks are minimized, and benefits outweigh any potential harm.

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The institutional review board (IRB) is responsible for reviewing research studies involving human subjects to ensure ethical standards are met.
Researchers conducting studies involving human subjects are required to file with the institutional review board (IRB).
To fill out the institutional review board application, researchers must provide detailed information about the study protocol, risks and benefits, and informed consent procedures.
The purpose of the institutional review board (IRB) is to protect the rights and welfare of human research participants.
The institutional review board application must include information on the study design, risks and benefits, informed consent process, and qualifications of researchers.
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