History of the Food and Drug Administration information

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...

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...

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

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

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...

The United States Food and Drug Administration Modernization Act of 1997 (FDAMA) amended the Federal Food, Drug, and Cosmetic Act. This act is related...

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

Food and Drug Safety and its six regional offices were established. It was raised to the status of administration (Korea Food & Drug Administration)...

the portion of the Code of Federal Regulations that governs food and drugs within the United States for the Food and Drug Administration (FDA), the Drug...

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

The Prescription Drug User Fee Act (PDUFA) was a law passed by the United States Congress in 1992 which allowed the Food and Drug Administration (FDA)...

President of the United States George W. Bush signed the Food and Drug Administration Amendments Act of 2007 (FDAAA) on September 27, 2007. This law reviewed...

The Center for Food Safety and Applied Nutrition (CFSAN (/ˈsɪfˌsæn/ SIF-san)) is the branch of the United States Food and Drug Administration (FDA) that...

The Food and Drug Administration's (FDA) New Drug Application (NDA) is the vehicle in the United States through which drug sponsors formally propose that...

Title 21 of the United States Code governs Food and Drugs in the United States Code (U.S.C.). Title 21 has 26 chapters: 21 U.S.C. ch. 1 — Adulterated...

The Food Safety Modernization Act (FSMA) was signed into law by President Barack Obama on January 4, 2011. The FSMA has given the Food and Drug Administration...

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

The Center for Drug Evaluation and Research (CDER, pronounced "see'-der") is a division of the U.S. Food and Drug Administration (FDA) that monitors most...

regulatory practice, the PDUFA date is the colloquial name for the date by which the Food and Drug Administration must respond to a New Drug Application or...

in the Legalization Debate". Science. 278 (5335): 47–52. doi:10.1126/science.278.5335.47. PMID 9311925. History of the Food and Drug Administration. Retrieved...

the 25th Commissioner of the Food and Drug Administration. He was first nominated to be commissioner in September 2015 by President Barack Obama and he...

Drugs are typically distinguished from food and other substances that provide nutritional support. Consumption of drugs can be via inhalation, injection, smoking...

The history of early food regulation in the United States started with the 1906 Pure Food and Drug Act, when the United States federal government began...

(AAAS) and co-chair of the InterAcademy Partnership (IAP). She served as the 21st Commissioner of the U.S. Food and Drug Administration from May 2009 to...