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This document outlines the procedures and policies for the Institutional Review Board (IRB) at Judson University, emphasizing the protection of human subjects in research conducted under its auspices.
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How to fill out Judson University Institutional Review Board Procedures and Policies

01
Begin by reviewing the Judson University IRB Procedures and Policies document thoroughly.
02
Identify the purpose of your research and determine whether it requires IRB review.
03
Gather all necessary documents, such as research proposals, consent forms, and recruitment materials.
04
Complete the IRB application form accurately, providing detailed information about your study.
05
Include information on potential risks and benefits to participants.
06
Ensure that you provide a clear description of participant recruitment methods.
07
Submit any additional supporting documents as required by the IRB.
08
Await confirmation of receipt from the IRB and respond to any requests for clarification or additional information.
09
Once approved, follow the guidelines for conducting your research as outlined in the approval letter.

Who needs Judson University Institutional Review Board Procedures and Policies?

01
All researchers conducting studies involving human participants at Judson University.
02
Faculty members who are leading research projects.
03
Students undertaking research as part of their academic programs.
04
Any external researchers collaborating with Judson University on research involving human subjects.
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§ 56.111 Criteria for IRB approval of research. In evaluating risks and benefits, the IRB should consider only those risks and benefits that may result from the research (as distinguished from risks and benefits of therapies that subjects would receive even if not participating in the research).
IRB Review Process: The IRB review process is in place to protect the rights and welfare of humans participating as subjects in research studies. IRB approval is required when research involving human subjects: Receives federal funds either directly or indirectly. Takes place at a university or hospital.
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.
IRB Process Submission of Research Proposal: Researchers submit their research proposal to the IRB. Initial Review: Exemption Determination (if applicable): Expedited Review (if applicable): Full Board Review (if applicable): Approval Decision: Ongoing Oversight:
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.
IRB – Principles Respect for Persons. Acknowledgement of the autonomy of the individual and the responsibility to provide special protection for individuals with reduced autonomy. Beneficence. A responsibility to do no harm, to maximize possible benefits, and to minimize possible harm. Justice.

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Judson University Institutional Review Board Procedures and Policies are guidelines that govern the ethical review of research involving human subjects to ensure compliance with federal regulations and to protect the rights and welfare of participants.
All faculty, staff, and students involved in research projects that involve human subjects at Judson University are required to file these procedures and policies.
To fill out the procedures and policies, researchers must complete the IRB application form, provide a detailed description of the research project, including methodology and participant recruitment, and submit any necessary supporting documents.
The purpose is to ensure ethical standards are maintained in research involving human subjects, to ensure participant safety, and to ensure compliance with legal and institutional regulations.
Researchers must report the research project title, principal investigator information, a summary of the research, recruitment methods, informed consent process, risk assessment, and any potential benefits to participants.
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