Glossary

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Term of the Day

Informed consent

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.

F

Food and Drug Administration (FDA)

The Food and Drug Administration (FDA), an US administration, is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the safety of the nation's food supply, cosmetics, and products that emit radiation. The FDA has regulatory responsabilities, it enforces laws and regulations. It also produces guidance documents. It approves products, can organize recalls, market withdrawals, and safety alerts. 

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