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Wichita State University Institutional Review Board (IRB) Research Project Continuation Form IRB #:Approval Expiration Date:Date of this Report:Title of Research Study: Principal Investigator(s): Department: Email
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How to fill out institutional review board irb

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How to fill out institutional review board irb

01
Step 1: Read and understand the guidelines and regulations set by the Institutional Review Board (IRB).
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Step 2: Begin by filling out the required administrative information such as the project title, investigator's name, department, and contact details.
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Step 3: Provide a clear and concise description of the research project, including the objectives, methods, and expected outcomes.
04
Step 4: Identify and address any potential risks and benefits associated with the research. This may involve discussing the procedures, participant population, and any necessary safeguards.
05
Step 5: Outline the informed consent process and document how you will obtain and manage consent from participants. Explain how you will protect participant confidentiality.
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Step 6: Include any supporting materials such as survey questionnaires, interview guides, or consent forms as required by the IRB.
07
Step 7: Review and revise the completed IRB form for accuracy and completeness.
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Step 8: Submit the filled-out IRB form, along with any required documents, to the designated IRB review board for evaluation and approval.
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Step 9: Cooperate with the IRB review process, addressing any feedback or concerns they may have.
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Step 10: Upon receiving IRB approval, you may proceed with your research project while adhering to any stipulations or guidelines outlined by the IRB.

Who needs institutional review board irb?

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Any individual or organization planning to conduct research involving human subjects usually needs to obtain institutional review board (IRB) approval. This requirement applies to academic researchers, medical professionals, psychologists, social scientists, and other professionals. Additionally, both private and public institutions, such as universities, hospitals, and research facilities, are typically required to have an IRB process in place.
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The Institutional Review Board (IRB) is a committee responsible for reviewing research studies involving human subjects to ensure their ethical treatment and compliance with regulations.
Researchers conducting studies involving human subjects are required to file for Institutional Review Board (IRB) approval.
To fill out an Institutional Review Board (IRB) application, researchers must provide detailed information about the study protocol, risks and benefits to participants, and procedures for obtaining informed consent.
The purpose of the Institutional Review Board (IRB) is to protect the rights and welfare of human subjects participating in research studies.
The Institutional Review Board (IRB) application requires detailed information about the study design, recruitment process, data collection methods, and potential risks and benefits to participants.
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