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This document is an application form to request review from the Committee for the Protection of Human Subjects at CSUS for a research project examining women's experiences in professional football,
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How to fill out Request for Review by the CSUS Committee for the Protection of Human Subjects

01
Obtain the 'Request for Review' form from the CSUS Committee's website or designated office.
02
Carefully read the instructions provided with the form to understand what information is required.
03
Fill out the form by providing your contact information, project title, and any applicable grant or funding information.
04
Describe the purpose of your research, including the significance and objectives.
05
Clearly outline the methodology, including participant recruitment, data collection methods, and any interventions.
06
Explain how you will ensure the confidentiality and privacy of participants.
07
Provide information on the potential risks to participants and how you plan to minimize them.
08
Include details about informed consent procedures.
09
Review the completed form for accuracy and completeness.
10
Submit the form by the specified deadline, following any additional submission protocols outlined by the committee.

Who needs Request for Review by the CSUS Committee for the Protection of Human Subjects?

01
Researchers conducting studies involving human subjects at CSUS.
02
Faculty members seeking to ensure compliance with ethical standards in their research.
03
Students engaged in research projects that involve human participants.
04
Any individual or group requiring approval for research involving interaction, intervention, or data collection from human subjects.
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Human subjects protection review board is a group of people who review, approve, and monitor the clinical study's protocol. Their role is to protect the rights and welfare of people participating in a study (referred to as human research subjects), such as reviewing the informed consent form.
This group review serves an important role in the protection of the rights and welfare of human research subjects. 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.
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.
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.
Institutional Review Board (IRB) The primary purpose of the IRB is to protect the rights and welfare of human subjects involved in research activities being conducted under its authority.
CPHS serves as the institutional review board (IRB) for CalHHS. The role of the CPHS (and other IRBs) is to ensure that research involving human subjects is conducted ethically and with minimal risk to participants.
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.

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The Request for Review is a formal application that researchers submit to the CSUS Committee for the Protection of Human Subjects to evaluate proposed research projects involving human participants, ensuring compliance with ethical standards and regulations.
Any faculty member, staff, or student conducting research involving human subjects at CSUS is required to file a Request for Review with the Committee.
To fill out the Request for Review, researchers must complete the appropriate forms provided by the Committee, detailing their research proposal, methodologies, participant recruitment strategies, and strategies for ensuring participant confidentiality and safety.
The purpose is to protect the rights and welfare of research participants, while ensuring that research involving human subjects is conducted ethically and in compliance with governmental regulations.
Researchers must report information including the study's title, objectives, participant demographics, methodology, informed consent process, risk assessment, and how data will be managed and protected.
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