Informed consent is the process of individuals agreeing to medical procedures or study participation after being fully informed. It involves detailing procedure information, risks, benefits, rights to decline, and confidentiality limits.
Informed consent is the process by which individuals agree to have a medical procedure or participate in a study after being informed of all relevant details that could impact their decision.
Obtaining informed consent involves providing information about the procedure, potential risks and benefits, the right to decline participation, consequences of withdrawal, and any legal confidentiality limits.
It is essential in research to ensure that participants provide informed consent voluntarily and with a full understanding of the research and its implications.
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