Informed consent is a legal and ethical concept that requires individuals to fully understand the risks, benefits, and alternatives of a particular decision or action before providing their consent. In medical contexts, it entails healthcare providers disclosing relevant information to patients about proposed treatments or procedures, including potential risks and expected outcomes. Informed consent ensures that individuals have the autonomy to make decisions about their own health and well-being based on accurate and comprehensive information. It is a fundamental principle in medical ethics and is also applicable in other areas such as research participation, legal agreements, and business transactions.
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This glossary post was last updated: 29th March 2024.
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