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INSTITUTIONAL REVIEW BOARD AUTHORIZATION AGREEMENT This Institutional Review Board Authorization Agreement (this Agreement), by and between the University of Southern California, a California nonprofit
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How to fill out this institutional review board

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How to fill out this institutional review board

01
Start by gathering all the necessary documents and forms required by the institutional review board (IRB) of your institution.
02
Carefully review the instructions and guidelines provided by the IRB to understand the process and any specific requirements.
03
Begin filling out the IRB application form by providing your personal information, such as name, contact details, and institutional affiliations.
04
Clearly describe the research study or project that requires IRB approval. Include details about the purpose, methodology, participants, and any potential risks or benefits.
05
Attach any supporting documents, such as research protocols, consent forms, questionnaires, or recruitment materials as per the IRB guidelines.
06
Review your filled out application thoroughly to ensure all necessary information is included and that it adheres to the IRB's ethical and regulatory standards.
07
Submit the completed application along with all supporting documents to the designated IRB submission portal or office.
08
Wait for the IRB to review your application. They may request additional information or revisions if needed.
09
If your application is approved, you will receive an official notification from the IRB. Follow any further instructions provided.
10
If your application is not approved, carefully review the feedback provided by the IRB and make necessary revisions or address any concerns raised.
11
Repeat the submission process with the revised application if required, ensuring to address any concerns raised by the IRB.
12
Once your research study or project is complete, follow any reporting or closure requirements specified by the IRB.

Who needs this institutional review board?

01
Institutional review boards (IRBs) are typically required by academic institutions, research organizations, and any entity conducting research involving human subjects.
02
Researchers, scientists, students, and other individuals or groups planning to conduct studies or projects involving human subjects may need to seek IRB approval.
03
Funding agencies and regulatory bodies may also require IRB approval before providing financial support or granting necessary permits for research involving human subjects.

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The institutional review board (IRB) is a committee responsible for reviewing and approving research involving human subjects to ensure that the research is conducted ethically.
Researchers conducting studies involving human subjects are required to submit their research protocols to the institutional review board for approval.
Researchers need to complete the necessary forms and provide detailed information about their research protocols, including the procedures for obtaining informed consent from participants.
The purpose of the institutional review board is to protect the rights and welfare of human research subjects by ensuring that research is conducted ethically and in compliance with regulations.
Researchers must report details about the research protocol, participant recruitment methods, informed consent procedures, and plans for data collection and analysis.
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