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FOR OFFICE USE ONLY IRB Protocol # Type of Review Requested: Exempt Status (see RR 101) Expedited Full Boarder details regarding types of review, please see Levels of Review under FAQ at www.seu.edu/irb
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How to fill out request for irb review

01
Start by gathering all necessary documentation and information required for the IRB review.
02
Begin by writing a cover letter for your request, including your contact information and a brief introduction about the purpose of the research.
03
Clearly state the objective or research question you aim to address with your study.
04
Provide a detailed description of your research design, including the methods and procedures you plan to use.
05
Include information on the target population or sample size you will be working with.
06
Discuss any potential risks or benefits for participants involved in the study.
07
Describe how you plan to obtain informed consent from participants and ensure their privacy and confidentiality.
08
Include any supporting documents such as informed consent forms, interview guides, questionnaires, or study protocols.
09
Specify any funding sources or conflicts of interest that may exist.
10
Conclude your request by expressing your willingness to address any concerns or questions raised by the IRB reviewers and provide your signature.
11
Review and proofread your request for any grammatical or formatting errors before submission.
12
Submit your completed request for IRB review through the designated submission process.

Who needs request for irb review?

01
Researchers or individuals conducting research involving human subjects need to submit a request for IRB review. This includes researchers from academic institutions, medical professionals, and individuals conducting independent research.
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Request for IRB review is a formal submission that researchers make to the Institutional Review Board (IRB) in order to obtain approval for their research involving human subjects.
Researchers who are conducting research involving human subjects are required to file a request for IRB review.
Researchers can fill out a request for IRB review by providing detailed information about their research protocol, potential risks to participants, informed consent process, and confidentiality measures.
The purpose of request for IRB review is to ensure that research involving human subjects is conducted ethically and with the protection of participants' rights and welfare.
Request for IRB review must include information about the research protocol, potential risks to participants, informed consent process, and confidentiality measures.
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