Aug 20, 2021 · The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological …
FDA stands for the Food and Drug Administration, a government agency responsible for the safety of food, dietary supplements, human drugs, vaccines, blood products and other biologicals, medical devices, radiation-emitting electronics, cosmetics, veterinarian products and tobacco products being sold or manufactured in the United States.What does FDA mean in medical terms?
medical device. FDA. Any article or healthcare product intended for use in the diagnosis of disease or other condition, or for use in the care, treatment or prevention of disease, which does not achieve any of its primary intended purposes by chemical action or by being metabolised.What is the role of FDA?
The Food and Drug Administration (FDA) is a U.S. government agency within the Department of Health and Human Services. The primary role of the FDA is protecting public health by ensuring the safety and effectiveness of drugs, vaccines, medical devices and food products.Why was FDA established?
How it came to be. The FDA got its start with the passage of the country’s first major food and drug safety bill, the 1906 Pure Food and Drug Act. That law's origins stem from a decades-long fight for the government to regulate food.
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