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This document outlines the application process for conducting research involving human subjects at Cal Poly Pomona, detailing ethical considerations, research design, data collection, and participant
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How to fill out Cal Poly Pomona - Human Research Protections Program Institutional Review Board (IRB) Protocol Application
01
Download the IRB Protocol Application form from the Cal Poly Pomona website.
02
Read the guidelines and instructions provided for filling out the application.
03
Provide your contact information including name, department, and email address.
04
Clearly state the purpose of your research project.
05
Outline your research methodology, including participant recruitment, data collection, and analysis.
06
Describe any potential risks to participants and how you will mitigate them.
07
Include a detailed plan for obtaining informed consent from participants.
08
Specify the duration of the study and the number of participants involved.
09
Submit any supporting documents such as consent forms and survey instruments.
10
Review all information for completeness and accuracy before submitting the application.
Who needs Cal Poly Pomona - Human Research Protections Program Institutional Review Board (IRB) Protocol Application?
01
Researchers conducting studies involving human subjects at Cal Poly Pomona.
02
Faculty and staff members looking to ensure compliance with ethical research standards.
03
Students engaging in research that requires human participant involvement.
04
Any individuals planning to collect data from human participants on campus.
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People Also Ask about
What are the minimum requirements for an IRB protocol?
An IRB must: have at least five members with varying backgrounds to promote complete and adequate review of the research activities commonly conducted by the institution; make every nondiscriminatory effort to ensure that the membership is not composed of entirely men or entirely women;
What happens if you don't get IRB approval?
Under 45 CFR 46.103, the IRB must review and approve all non-exempt human subject research. Failure to obtain IRB approval before conducting research could result in the researcher being unable to use data and other information collected through the research process.
What are the ethical requirements for IRB?
The IRB expects that personnel who are involved in the consent process, other aspects of human subject protection, or handling private health information will also be listed.
What are the minimum elements that are typically required for an IRB protocol?
Research Requiring Comprehensive IRB Review Risks to the subjects are minimal, and are reasonable in relation to anticipated benefits. The subject selection is equitable. Privacy and confidentiality are protected. Informed consent processes meet federal regulatory and U-M requirements.
What are the requirements for an IRB?
The IRB must review the following requirements in order to give approval to research: 1) the risks are rational and minimized in relation to the anticipated benefits to the subjects based on a risk/benefit analysis; 2) the choice of subjects is equitable; 3) informed consent is obtained from each potential subject or a
What goes into an IRB application?
Before completing the IRB application form, you must know: • The identity of all of the investigators who will be working on the project; • Who will be recruited to participate and how they will be recruited; • Where the research will be conducted; • What data will be collected and what will happen to that data; • How
What 5 types of people must be present at an institutional review board?
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.
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What is Cal Poly Pomona - Human Research Protections Program Institutional Review Board (IRB) Protocol Application?
The Cal Poly Pomona - Human Research Protections Program Institutional Review Board (IRB) Protocol Application is a formal document that researchers must submit to obtain approval for conducting research involving human subjects. This application ensures that the research complies with ethical standards and federal regulations protecting the rights and welfare of participants.
Who is required to file Cal Poly Pomona - Human Research Protections Program Institutional Review Board (IRB) Protocol Application?
Any faculty, staff, or student at Cal Poly Pomona who intends to conduct research involving human subjects is required to file the IRB Protocol Application. This includes all research projects, whether funded or unfunded.
How to fill out Cal Poly Pomona - Human Research Protections Program Institutional Review Board (IRB) Protocol Application?
To fill out the IRB Protocol Application, researchers should follow these steps: Download the application form from the Cal Poly Pomona IRB website, provide detailed information about the research project including objectives, methodology, participant recruitment, and consent processes, and ensure all sections are completed accurately before submitting the application.
What is the purpose of Cal Poly Pomona - Human Research Protections Program Institutional Review Board (IRB) Protocol Application?
The purpose of the IRB Protocol Application is to protect the rights and welfare of human research participants by ensuring that research is conducted ethically and in compliance with federal regulations. It also facilitates the review process to ensure that risks to participants are minimized and that informed consent is obtained.
What information must be reported on Cal Poly Pomona - Human Research Protections Program Institutional Review Board (IRB) Protocol Application?
The information that must be reported includes the researcher's details, a description of the research project, the study design and methodology, participant demographics, recruitment strategies, potential risks and benefits, data collection methods, and the informed consent process.
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