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This document is used to request review by the Sacramento State Committee for the Protection of Human Subjects regarding a research project involving physics majors as learning assistants in astronomy
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How to fill out Request for Review by the Sacramento State Committee for the Protection of Human Subjects

01
Obtain the Request for Review form from the Sacramento State Committee for the Protection of Human Subjects website.
02
Fill in the title of your research project at the top of the form.
03
Provide your contact information, including your name, department, and email address.
04
Clearly describe the purpose of your research and how it involves human subjects.
05
Detail the methodologies you will use to collect data, including recruitment procedures for participants.
06
Explain the potential risks to participants and how you will mitigate them.
07
Describe how participants' confidentiality will be protected.
08
Include information about informed consent and how you will obtain it from participants.
09
Review all sections of the form to ensure completeness and accuracy.
10
Submit the completed form to the committee along with any supporting documents required.

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

01
Researchers conducting studies that involve human subjects at Sacramento State University.
02
Faculty, staff, or students planning research projects that require ethical review and approval.
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People Also Ask about

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.
The Institutional Review Board (IRB) is an administrative body established to protect the rights and welfare of human research subjects recruited to participate in research activities conducted under the auspices of the institution with which it is affiliated.
The NSF version of Code of Federal Regulations 45 CFR 690.101-124 gives grantee institutions the responsibility for setting up "Institutional Review Boards," or IRBs. These boards review research protocols and designs and ensure the rights of human subjects are protected.
An IRB is a committee — operating under federal regulations, state laws and institutional policy — that reviews research involving human subjects to ensure the ethical and equitable treatment of those subjects.
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.
How to get IRB review Complete the Human Subjects Research TrainingThe Human Subjects Research course is required of all USC investigators and personnel on the IRB application. Submit an ISTAR ApplicationApplications for IRB review must be submitted online through the iStar system.
Institutional Review Boards (IRBs) assess the ethics and safety of research studies involving human subjects, such as behavioral studies or clinical trials for new drugs or medical devices.
Institutional review boards (IRBs) or research ethics committees provide a core protection for human research participants through advance and periodic independent review of the ethical acceptability of proposals for human research.

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The Request for Review by the Sacramento State Committee for the Protection of Human Subjects is a formal submission for assessing research proposals that involve human subjects to ensure compliance with ethical standards and regulations.
Researchers, faculty, or students at Sacramento State University conducting studies involving human subjects are required to file the Request for Review.
To fill out the Request for Review, researchers must complete the Application form provided by the committee, detailing the research purpose, methods, participant information, and ethical considerations involved.
The purpose is to ensure that the rights and welfare of human subjects are protected, and that all research complies with ethical standards and federal regulations.
Information required includes the research title, researcher details, study objectives, methodology, participant recruitment process, informed consent process, and measures for confidentiality and risk minimization.
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