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This document outlines the policies and procedures established by the Seattle Pacific University Institutional Review Board (IRB) to protect the rights, health, and privacy of individuals who participate
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How to fill out SPU Institutional Review Board Policies and Procedures

01
Gather all required information about your research project.
02
Review the SPU Institutional Review Board (IRB) Policies and Procedures document.
03
Complete the necessary forms provided by the IRB.
04
Clearly describe the purpose and methodology of your research.
05
Outline any potential risks to participants and how you will mitigate them.
06
Include a plan for obtaining informed consent from participants.
07
Submit the completed forms and research proposal to the IRB for review.
08
Respond to any feedback or requested revisions from the IRB.

Who needs SPU Institutional Review Board Policies and Procedures?

01
Researchers at SPU conducting studies involving human subjects.
02
Faculty members overseeing student research projects.
03
Students planning to conduct research that requires ethical review.
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People Also Ask about

IRBs are charged with providing an independent evaluation that proposed research is ethically acceptable, checking clinical investigators' potential biases, and evaluating compliance with regulations and laws designed to protect human subjects.
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.
There are three major types of review: Exempt, Expedited, and Full.
The U.S. Federal policy requires that an IRB have at least 5 members of varying backgrounds including a chair person, a scientific member, a non‐scientific member, a representative of the community not affiliated with the institution, and a member of the institution.
The IRB is concerned with protecting the welfare, rights, and privacy of human subjects. The IRB has the authority to approve, exempt, disapprove, monitor, and require modifications in all research activities that fall within its jurisdiction as specified by both the federal regulations and institutional policy.
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.
Under FDA regulations, an IRB is an appropriately constituted group that has been formally designated to review and monitor biomedical research involving human subjects. In ance with FDA regulations, an IRB has the authority to approve, require modifications in (to secure approval), or disapprove research.
The purpose of IRB review is to assure, both in advance and by periodic review, that appropriate steps are taken to protect the rights and welfare of humans participating as subjects in the research.

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The SPU Institutional Review Board (IRB) Policies and Procedures outline the guidelines and ethical standards for conducting research involving human subjects at Seattle Pacific University (SPU). These policies ensure compliance with federal regulations and protect the rights and welfare of participants.
Any faculty, staff, or student at SPU who is conducting research involving human subjects is required to file under the SPU Institutional Review Board Policies and Procedures.
To fill out the SPU IRB Policies and Procedures, researchers must complete the required application forms, provide detailed information about the research project, including its purpose, methodology, participant recruitment, informed consent process, and data protection measures, and submit these documents to the IRB for review.
The purpose of the SPU Institutional Review Board Policies and Procedures is to ensure that all research involving human subjects is conducted ethically, safeguarding participants' rights and welfare, ensuring informed consent, and maintaining compliance with applicable laws and regulations.
Researchers must report information such as the research objectives, study design, participant demographics, recruitment methods, data collection procedures, potential risks and benefits, consent process, and confidentiality measures on the SPU Institutional Review Board application.
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