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Informed consent is a process where a participant voluntarily agrees to take part in a research study after being informed of all aspects of the study.
Researchers or individuals conducting the research study are required to file informed consent.
Informed consent forms are typically filled out by providing clear and comprehensive information about the study, risks, benefits, confidentiality, and participant rights.
The purpose of informed consent is to ensure that participants are fully aware of what they are agreeing to and to protect their rights and safety during the research study.
Informed consent forms must include information about the study purpose, risks, benefits, confidentiality, voluntariness, and contact information for questions.
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