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

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...

Congress in the 20th century and led to the creation of the Food and Drug Administration. Its main purpose was to ban foreign and interstate traffic in adulterated...

Food and Drug Safety (MFDS; Korean: 식품의약품안전처; Hanja: 食品醫藥品安全處; RR: Sikpumuiyakpumanjeoncheo), formerly known as the Korea Food & Drug Administration (KFDA;...

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

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...

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

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...

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

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

Drugs@FDA. U.S. Food and Drug Administration (FDA). Retrieved 21 November 2019. "New Drug Application (NDA) 013263". Drugs@FDA. U.S. Food and Drug Administration...

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

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

of China Food and Drug Administration (FDA; Chinese: 食品藥物管理署) is a Republic of China government agency, which is responsible for the safety and quality...

Prescription Drug Marketing Act (PDMA). The Food and Drug Administration (FDA) is charged with implementing the law. As a general rule, over-the-counter drugs (OTC)...

and Drug Administration. 30 January 2018. Retrieved 18 April 2024. "FDA - Germany, MOU on Good Laboratory Practice". U.S. Food and Drug Administration. 31...

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

Food and Drug Administration v. Alliance for Hippocratic Medicine is a pending United States Supreme Court case to challenge the U.S. Food and Drug Administration...

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...

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...

The Drug Enforcement Administration (DEA) is a United States federal law enforcement agency under the U.S. Department of Justice tasked with combating...

The United States Food and Drug Administration's Investigational New Drug (IND) program is the means by which a pharmaceutical company obtains permission...

original weight within 5 years of stopping treatment. The US Food and Drug Administration (FDA) approved semaglutide based on evidence from seven clinical...

the United States Food and Drug Administration that regulates food, dietary supplements, and cosmetics, The Food and Drug Administration (United States)...

October 2014, the U.S. Food and Drug Administration (FDA) issued a black box warning that losartan can cause fetal toxicity, and should be discontinued...

modes of action, and/or are used to treat the similar diseases. The Food and Drug Administration (FDA) has worked on classifying and licensing new medications...