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Get the free OU HRPP Program – HSC Campus REVIEWER CHECKLIST FOR NEW STUDIES - ouhsc

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Este documento es una lista de verificación para revisores que evalúan nuevas propuestas de estudios en relación con la investigación de sujetos humanos. Incluye instrucciones y preguntas sobre
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How to fill out OU HRPP Program – HSC Campus REVIEWER CHECKLIST FOR NEW STUDIES

01
Gather all necessary documents related to the study such as the protocol, informed consent forms, and recruitment materials.
02
Fill out the checklist by reviewing each item carefully, ensuring that all relevant sections pertaining to the study are addressed.
03
Provide detailed descriptions for each section where applicable, particularly in areas concerning ethics, compliance, and participant safety.
04
Attach supporting documents as required by checklist items, ensuring they are clearly labeled.
05
Review the completed checklist for accuracy and completeness before submission.
06
Submit the checklist along with other IRB submission materials to the appropriate office.

Who needs OU HRPP Program – HSC Campus REVIEWER CHECKLIST FOR NEW STUDIES?

01
Researchers initiating new studies at the OU HSC Campus who require approval from the Institutional Review Board (IRB).
02
Faculty and staff involved in research that interacts with human subjects.
03
Students conducting research under the supervision of faculty members that requires ethical review.
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The OU HRPP Program – HSC Campus REVIEWER CHECKLIST FOR NEW STUDIES is a tool designed to ensure that new research studies involving human subjects meet all ethical and regulatory requirements before they are approved for initiation.
Principal investigators and research teams conducting new studies involving human subjects at the HSC Campus are required to file the OU HRPP Program – HSC Campus REVIEWER CHECKLIST FOR NEW STUDIES.
To fill out the checklist, researchers must carefully review each item listed, provide necessary information and documentation, and ensure that all requirements related to ethical research conduct are addressed before submission.
The purpose of the checklist is to facilitate a thorough review of new studies to protect the rights and welfare of participants and ensure compliance with institutional, federal, and state regulations.
Researchers must report information including study design, participant recruitment methods, informed consent processes, risk assessment, and data protection measures on the checklist.
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