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PREPARED FOR RADIATION ONCOLOGY FACULTY DEFINITIONS: IRB Forms 2, 2a, or 3 Consent to research Contains HIPAA language so that the consent document also serves as HIPAA authorization No active participation
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Form K1 IRB WUSTL is a form used by researchers at Washington University in St. Louis to request Institutional Review Board (IRB) approval for research projects involving human subjects.
Researchers conducting projects involving human subjects at Washington University in St. Louis are required to file Form K1 IRB WUSTL.
To fill out Form K1 IRB WUSTL, researchers need to provide detailed information about their research project, including the purpose, procedures, risks, and benefits. They also need to explain how they will ensure the protection of human subjects.
The purpose of Form K1 IRB WUSTL is to obtain Institutional Review Board approval for research projects involving human subjects and ensure that the rights and welfare of those subjects are protected.
Form K1 IRB WUSTL requires researchers to report information about the research project, including the study design, recruitment methods, data collection procedures, and plans for data analysis and storage. They also need to provide information about the potential risks and benefits for human subjects and the steps they will take to protect their rights and welfare.
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