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Interim Administrative Policy Responsible Official: Senior Vice President for Academic Affairs, Dean of the Faculty Effective Date: September 1, 2014, Use of Human Subjects in Research Interim Policy
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How to fill out use of human subjects:

01
Start by gathering all relevant information about the human subjects you intend to involve in your research. This includes their demographics, possible risks and benefits associated with their participation, and any necessary background information.
02
Next, carefully review your research protocol and ensure that it aligns with ethical standards and guidelines set forth by the relevant regulatory bodies, such as Institutional Review Boards (IRBs) or ethics committees. Make sure to address any ethical considerations, including informed consent, privacy protection, and potential risks to the subjects.
03
Begin filling out the necessary forms or applications provided by your institution or the regulatory body overseeing your research. These forms typically require detailed information about your research objectives, study design, methodology, and the process through which you will select and recruit human subjects.
04
Clearly articulate the inclusion and exclusion criteria for your study participants, ensuring that they are based on scientific justifications rather than discriminatory factors. The criteria should be fair and unbiased, and should aim to include a diverse sample of human subjects whenever possible.
05
Detail the informed consent process, which involves providing potential subjects with all necessary information about the study, including its purpose, procedures, potential benefits, and any known risks or discomforts. Ensure that the consent form is clear, concise, and easily understandable for the targeted population.
06
Describe the steps you will take to protect the privacy and confidentiality of your human subjects. This may involve assigning unique identification codes, storing data securely, and ensuring that only authorized individuals have access to personal information.
07
Outline any safeguards or measures you will implement to minimize potential risks to the human subjects. This may include regular monitoring, medical supervision, and provisions for medical treatment in case of adverse events.

Who needs use of human subjects?

01
Researchers in the fields of health sciences, social sciences, and psychology often require the use of human subjects to conduct studies and gather data relevant to their research objectives. This ensures that the findings are applicable to real-world situations and can be generalized to the larger population.
02
Institutions and organizations that fund research projects often have specific guidelines and regulations in place that require researchers to involve human subjects when conducting certain types of studies. This helps ensure that the research they fund is conducted in an ethical and responsible manner.
03
Regulatory bodies, such as Institutional Review Boards (IRBs) or ethics committees, play a crucial role in overseeing research involving human subjects. Their primary responsibility is to protect the rights, welfare, and well-being of the human subjects by reviewing and approving research protocols and ensuring that ethical standards are met.
04
In some cases, governmental agencies or policy-making bodies may require researchers to involve human subjects in their studies to address specific research questions or public health concerns. This helps inform evidence-based policies and decision-making processes.
Overall, the use of human subjects in research is important for advancing scientific knowledge, addressing societal issues, and ensuring that research is conducted ethically and responsibly.
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The use of human subjects is important for conducting research and experiments to gather data and information.
Researchers and institutions conducting experiments and research involving human subjects are required to file use of human subjects.
The use of human subjects form can typically be filled out online or through a paper form provided by the Institutional Review Board (IRB) or Ethics Committee.
The purpose of use of human subjects is to ensure that research involving human participants is ethical, safe, and complies with regulations.
Information such as the purpose of the study, risks and benefits to participants, informed consent procedures, and confidentiality measures must be reported on use of human subjects.
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