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Informed Consent in Human Subjects ResearchOffice for the Protection of Research Subjects (OPUS)Leon Tenure, M.S.W. Candidate Student Mentor Monica Baker Program Coordinator Katherine Hawthorne Program
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Who needs informed consent in?

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Informed consent is needed in various situations where individuals may undergo a procedure, participate in research, receive medical treatment, or engage in activities that may carry certain risks or implications.
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Some examples of who needs informed consent include patients before undergoing surgery, participants in clinical trials or research studies, individuals receiving experimental treatments, individuals participating in psychology experiments, and individuals involved in legal or contractual agreements.
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Informed consent is a process for getting permission to do something involving people's understanding of what will happen and what risks are involved.
Informed consent is typically filed by researchers, healthcare professionals, or anyone conducting a study or treatment involving human subjects.
To fill out informed consent, one must provide detailed information about the study or treatment, potential risks and benefits, confidentiality, and ensure that the participant understands and agrees to participate.
The purpose of informed consent is to protect the rights and well-being of participants in research studies or medical treatments by ensuring they understand the risks and benefits.
Informed consent forms typically include information about the study or treatment, potential risks, benefits, confidentiality, participant rights, and the researcher's contact information.
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