The United States Food and Drug Administration (FDA or US FDA) is a federal agency of the Department of Health and Human Services. The FDA is responsible...

The Food and Drug Administration (FDA) of the Philippines, formerly the Bureau of Food and Drugs (BFAD /ˈbiːfæd/; 1982–2009), is a health regulatory agency...

The Food and Drug Administration is a federal agency of the United States, formed in 1930. Up until the 20th century, there were few federal laws regulating...

Numerous governmental and non-governmental organizations have criticized the U. S. Food and Drug Administration for alleged excessive and/or insufficient regulation...

giving authority to the U.S. Food and Drug Administration (FDA) to oversee the safety of food, drugs, medical devices, and cosmetics. The FDA's principal...

Food and Drug Administration may refer to: China Food and Drug Administration (NMPA) Food and Drug Administration, a government agency in the United States...

The Food and Drug Administration (FDA; Chinese: 食品藥物管理署) is an agency of the Ministry of Health and Welfare of Taiwan, which is responsible for the safety...

Food and Drug Administration is a ministry of the Government of Maharashtra. The ministry is responsible for consumer protection and regulating food and...

United States Congress, and led to the creation of the Food and Drug Administration (FDA). Its main purpose was to ban foreign and interstate traffic in...

The National Agency for Food and Drug Administration and Control (NAFDAC) is a Nigerian federal agency under the Federal Ministry of Health that is responsible...

Food and Drug Administration, Maharashtra State, is Maharashtra's primary instrument of consumer protection. It is a law enforcement agency. In 1970, the...

The Food and Drug Administration Safety and Innovation Act of 2012 (FDASIA) is a piece of American regulatory legislation signed into law on July 9, 2012...

drug. A generic drug must contain the same active ingredients as the original brand-name formulation. The U.S. Food and Drug Administration (FDA) requires...

The Ministry of Food and Drug Safety (MFDS; Korean: 식품의약품안전처), formerly known as the Korea Food & Drug Administration (KFDA; 식품의약품안전청), is a government...

commissioner of food and drugs is the head of the Food and Drug Administration (FDA), an agency of the United States Department of Health and Human Services...

ISBN 978-0-86196-607-3. Retrieved 29 June 2024. "New Drug Application (NDA) 008943". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on...

The Department of Food and Drug Administration (Burmese: အစားအသောက်နှင့် ဆေးဝါးကွပ်ကဲရေး ဦးစီးဌာန; abbreviated FDA) is Burma's food safety regulatory...

State Administration for Market Regulation. The agency had multiple former names, including China Food and Drug Administration and State Food and Drug Administration...

The regulation of food and dietary supplements by the U.S. Food and Drug Administration is a process governed by various statutes enacted by the United...

semaglutide, and tirzepatide are approved by the US Food and Drug Administration (FDA) for weight management in combination with reduced-calorie diet and increased...

a significantly elevated risk of acute pancreatitis. The US Food and Drug Administration prescription label for semaglutide contains a boxed warning for...

Center for Food Safety and Applied Nutrition, Inspections, Compliance, Enforcement, and Criminal Investigations, US Food and Drug Administration. Retrieved...

The United States Food and Drug Administration Modernization Acts (FDAMA) are amendments to the Federal Food, Drug, and Cosmetic Act, which regulated...

The Food and Drug Administration Revitalization Act was introduced by the 101st Congress of the United States. Senator Orrin G. Hatch was the chairperson...

development and drug sales. In the U.S., the Elixir Sulfanilamide disaster led to the establishment of the Food and Drug Administration, and the 1938 Federal...

manufacture and sale of OTC substances are regulated by the Food and Drug Administration. The FDA requires that all "new drugs" obtain a New Drug Application...

(GRAS) and may be lawfully marketed and added to food products, but stevia leaf and crude extracts do not have GRAS or Food and Drug Administration (FDA)...

the label must bear a disclaimer that the Food and Drug Administration (FDA) "has not evaluated the claim" and that the dietary supplement product is not...

"Zevaskyn". U.S. Food and Drug Administration (FDA). 28 April 2025. Retrieved 7 July 2025. "Encelto". U.S. Food and Drug Administration. 1 October 2024...

regulatory agencies, such as the European Food Safety Authority (EFSA) and US Food and Drug Administration (FDA), and by international reviewers, such as the...