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This document outlines the procedures and policies established by the Institutional Review Board at Southern Arkansas University to ensure the protection of human participants involved in research,
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How to fill out SAU IRB Guidelines

01
Read the SAU IRB Guidelines thoroughly to understand the requirements.
02
Identify the type of research you are conducting and determine if it falls under the IRB review.
03
Prepare an application form following the instructions in the guidelines.
04
Gather all necessary documents, including informed consent forms and research protocols.
05
Complete the application form by filling in all required fields accurately.
06
Review your application for completeness and accuracy before submission.
07
Submit the application to the IRB for review by the specified deadline.
08
Respond promptly to any requests for clarification or additional information from the IRB.

Who needs SAU IRB Guidelines?

01
Faculty members conducting research involving human participants.
02
Graduate and undergraduate students engaged in academic research.
03
Any staff member involved in research projects requiring ethical review.
04
External researchers collaborating with SAU on studies involving human subjects.
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There are three types of IRB review outlined in the federal regulations: Exempt Status, Expedited and Full Board review. The UI IRB reviews HawkIRB applications at the lowest level of regulatory oversight allowed by the Code of Federal Regulations for the Protection of Human Subjects (45 CFR 46).
Both IRB (Institutional Review Board) and IEC serve a similar purpose: to protect human subjects in research. But the difference between IRB and IEC lies mainly in geography and terminology.
There are three levels of IRB review for human subjects' research: exempt, expedited , and convened. Institutional policy requires IRB review of all human subjects' research that falls into an exempt or expedited review category.
When reviewing research, Institutional Review Board (IRB) members are guided by three ethical principles that are fundamental to human participant protection: respect for persons, beneficence, and justice.
All proposals submitted for either expedited or full review must contain four primary sections: Purpose of investigation and procedures. Anticipated risk and potential benefits to participants. Steps taken to protect the participants. Manner of obtaining participants.
IRB must review all projects that meet the definition of research and that involve human subjects prior to any data collection to determine the appropriate level of review, and, as appropriate, approve them. There are three major types of review: Exempt, Expedited, and Full.
When reviewing research, Institutional Review Board (IRB) members are guided by three ethical principles that are fundamental to human participant protection: respect for persons, beneficence, and justice.
Human subject research is categorized in one of three classifications based on the level of risk. These classifications include full board review, expedited review, and exempt status.

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SAU IRB Guidelines refer to the set of rules and procedures established by the Southern Arkansas University Institutional Review Board (IRB) to ensure that research involving human subjects is conducted ethically and complies with federal regulations.
All researchers, including faculty, staff, and students at Southern Arkansas University conducting research involving human subjects, are required to file under the SAU IRB Guidelines.
Researchers must complete an application form that outlines their research project, including the purpose, methodology, and how they will obtain consent from participants. Detailed instructions are provided by the IRB office.
The purpose of SAU IRB Guidelines is to protect the rights and welfare of human subjects involved in research, ensuring ethical standards are upheld and participants are treated with respect and care.
Researchers must report information including research objectives, participant selection criteria, informed consent process, risk assessment, data confidentiality measures, and plans for data analysis.
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