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Informed consent is a principle in medical ethics, medical law and media studies, that a patient must have sufficient information and understanding before making decisions about their medical care.
Jun 5, 2023 · Informed consent is the process in which a health care provider educates a patient about the risks, benefits, and alternatives of a given procedure or intervention. The patient must be competent to make a voluntary decision about whether to undergo the procedure or intervention.
- 2023/06/05
Dec 7, 2015 · Learn what informed consent means in different situations, such as medical, legal, and contractual contexts. Find out the legal requirements, risks, and benefits of obtaining and giving informed consent.
Oct 11, 2019 · Informed consent is a process that lets you decide which medical treatments you want or don't want. Learn what it is, when it's needed, what it should include, and why it's important for your health and well-being.
Mar 2, 2017 · Informed consent, which is ethically essential in most clinical research, respects persons’ rights to decide whether participation in the research is compatible with their interests, including...
An “Informed” consent emphasizes a process where the clinical research participant must receive and comprehend information appropriately to make an autonomous decision.
Informed consent is an ethical and legal requirement for research involving human participants.
