Food and Drug Administration

FDAU.S. Food and Drug AdministrationUnited States Food and Drug AdministrationUS Food and Drug AdministrationUS FDAFood and Drug Administration (FDA)USFDAU.S. FDAFood & Drug AdministrationU.S. Food & Drug Administration
The Food and Drug Administration (FDA or USFDA) is a federal agency of the United States Department of Health and Human Services, one of the United States federal executive departments.wikipedia
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Federal Food, Drug, and Cosmetic Act

Food, Drug, and Cosmetic ActFood, Drug and Cosmetic ActFederal Food, Drug and Cosmetic Act
The FDA was empowered by the United States Congress to enforce the Federal Food, Drug, and Cosmetic Act, which serves as the primary focus for the Agency; the FDA also enforces other laws, notably Section 361 of the Public Health Service Act and associated regulations, many of which are not directly related to food or drugs.
The United States Federal Food, Drug, and Cosmetic Act (abbreviated as FFDCA, FDCA, or FD&C), is a set of laws passed by Congress in 1938 giving authority to the U.S. Food and Drug Administration (FDA) to oversee the safety of food, drugs, medical devices, and cosmetics.

Commissioner of Food and Drugs

CommissionerFDA commissionerCommissioner of the Food and Drug Administration
The FDA is led by the Commissioner of Food and Drugs, appointed by the President with the advice and consent of the Senate.
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 and Human Services.

Tobacco

tobacco leavessnufftobacco leaf
The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices (ERED), cosmetics, animal foods & feed and veterinary products.
In the 1990s, this prompted the Food and Drug Administration to use this strain as evidence that tobacco companies were intentionally manipulating the nicotine content of cigarettes.

Center for Biologics Evaluation and Research

CBERBureau of BiologicsCenter for Biologics Evaluation and Research (CBER)
The Center for Biologics Evaluation and Research is the branch of the FDA responsible for ensuring the safety and efficacy of biological therapeutic agents.
The Center for Biologics Evaluation and Research (CBER) is one of six main centers for the U.S. Food and Drug Administration (FDA), which is a part of the U.S. Department of Health and Human Services.

Center for Drug Evaluation and Research

CDERUS
The Center for Drug Evaluation and Research uses different requirements for the three main drug product types: new drugs, generic drugs, and over-the-counter drugs.
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 drugs as defined in the Food, Drug, and Cosmetic Act.

Center for Food Safety and Applied Nutrition

Bad Bug BookCenter for Food Safety and NutritionCFSAN
Cosmetics are regulated by the Center for Food Safety and Applied Nutrition, the same branch of the FDA that regulates food.
The Center for Food Safety and Applied Nutrition (CFSAN, pronounced sif'-san) is the branch of the United States Food and Drug Administration (FDA) that regulates food, dietary supplements, and cosmetics.

White Oak, Maryland

White OakWhite Oak, MDBurnt Mills
The FDA has its headquarters in unincorporated White Oak, Maryland.
The headquarters of the Food and Drug Administration now occupies the property, which has been renamed the Federal Research Center at White Oak.

Over-the-counter drug

over-the-counterover the counterOTC
The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices (ERED), cosmetics, animal foods & feed and veterinary products.
In the United States, the manufacture and sale of OTC substances are regulated by the Food and Drug Administration.

Medical device

medical devicesmedical equipmentmedical instrument
The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices (ERED), cosmetics, animal foods & feed and veterinary products. The Center for Devices and Radiological Health (CDRH) is the branch of the FDA responsible for the premarket approval of all medical devices, as well as overseeing the manufacturing, performance and safety of these devices.
The US FDA also published a series of guidances for industry regarding this topic against 21 CFR 820 Subchapter H—Medical Devices.

United States Department of Health and Human Services

Department of Health and Human ServicesU.S. Department of Health and Human ServicesHealth and Human Services
The Food and Drug Administration (FDA or USFDA) is a federal agency of the United States Department of Health and Human Services, one of the United States federal executive departments.
The six major program-operating components of the new Department were the Public Health Service, the Office of Education, the Food and Drug Administration, the Social Security Administration, the Office of Vocational Rehabilitation, and St. Elizabeth's Hospital.

Office of Criminal Investigations

OCIFDA's Office of Criminal InvestigationsUnited States Food and Drug Administration Office of Criminal Investigations
While most of the Centers are located in the Washington, D.C. area as part of the Headquarters divisions, two offices – the Office of Regulatory Affairs (ORA) and the Office of Criminal Investigations (OCI) – are primarily field offices with a workforce spread across the country.
The Office of Criminal Investigations (OCI) was established to provide the U.S. Food and Drug Administration (FDA) with a specific Office to conduct and coordinate Criminal investigations.

Naval Ordnance Laboratory

US Naval Ordnance LaboratoryNaval Ordinance LaboratoryNaval Surface Weapons Center
In recent years, the agency began undertaking a large-scale effort to consolidate its 25 operations in the Washington metropolitan area, moving from its main headquarters in Rockville and several fragmented office buildings to the former site of the Naval Ordnance Laboratory in the White Oak area of Silver Spring, Maryland.
The headquarters of the United States Food and Drug Administration (FDA) now occupies part of the former NOL.

Office of In Vitro Diagnostics and Radiological Health

Center for Devices and Radiological HealthCDRHbranch
The Center for Devices and Radiological Health (CDRH) is the branch of the FDA responsible for the premarket approval of all medical devices, as well as overseeing the manufacturing, performance and safety of these devices.
The Center for Devices and Radiological Health (CDRH) is the branch of the United States Food and Drug Administration (FDA) responsible for the premarket approval of all medical devices, as well as overseeing the manufacturing, performance and safety of these devices.

United States Secretary of Health and Human Services

Secretary of Health and Human ServicesSecretary of Health, Education, and WelfareU.S. Secretary of Health and Human Services
The Commissioner reports to the Secretary of Health and Human Services.
The Department of Health and Human Services oversees 11 agencies including the Food and Drug Administration (FDA), Center for Disease Control (CDC), National Institutes of Health (NIH), Administration for Children and Families (ACF) and Centers for Medicare & Medicaid Services (CMS).

Center for Veterinary Medicine

CVM
The Center for Veterinary Medicine (CVM) is a center of the FDA that regulates food additives and drugs that are given to animals.
The Center for Veterinary Medicine (CVM) is a branch of the U.S. Food and Drug Administration (FDA) that regulates the manufacture and distribution of food, food additives, and drugs that will be given to animals.

Office of Global Regulatory Operations and Policy

Office of Regulatory AffairsOffice of Medical Products and Tobacco
The Office of Global Regulatory Operations and Policy (GO), also known as the Office of Regulatory Affairs (ORA), is the part of the U.S. Food and Drug Administration (FDA) enforcing the federal laws governing biologics, cosmetics, dietary supplements, drugs, food, medical devices, radiation-emitting electronic devices, tobacco products, and veterinary medicine products which may have potentially harmful side effects for the consumer.

Controlled Substances Act

Schedule ISchedule IISchedule III
Other significant laws enforced by the FDA include the Public Health Service Act, parts of the Controlled Substances Act, the Federal Anti-Tampering Act, as well as many others.
Two federal agencies, the Drug Enforcement Administration (DEA) and the Food and Drug Administration (FDA), determine which substances are added to or removed from the various schedules, although the statute passed by Congress created the initial listing.

Silver Spring, Maryland

Silver SpringSilver Spring, MDdowntown Silver Spring
In recent years, the agency began undertaking a large-scale effort to consolidate its 25 operations in the Washington metropolitan area, moving from its main headquarters in Rockville and several fragmented office buildings to the former site of the Naval Ordnance Laboratory in the White Oak area of Silver Spring, Maryland.
Silver Spring's notable landmarks include the AFI Silver Theatre, the world headquarters of the Seventh-day Adventist Church, the headquarters of the National Oceanic and Atmospheric Administration, the headquarters of the Food and Drug Administration, and the national headquarters of the Ahmadiyya Muslim Community.

National Center for Toxicological Research

National Center for Toxicological Research (NCTR)
The National Center for Toxicological Research (NCTR) is the branch of the United States Food and Drug Administration which conducts research to define biological mechanisms of action underlying the toxicity of products regulated by the FDA.

Form FDA 483

FDA 483Form 483483
The U.S. Food and Drug Administration (FDA) is authorized to perform inspections under the Federal Food, Drug, and Cosmetic Act, Sec.

U.S. Customs and Border Protection

Customs and Border ProtectionUnited States Customs and Border ProtectionUS Customs and Border Protection
The FDA frequently works with other federal agencies, including the Department of Agriculture, Drug Enforcement Administration, Customs and Border Protection, and Consumer Product Safety Commission.
CBP also works with the U.S. Food and Drug Administration to screen high-risk imported food shipments in order to prevent bio-terrorism and agro-terrorism.

Prescription drug

prescriptionprescription drugsprescription medication
The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices (ERED), cosmetics, animal foods & feed and veterinary products.
The Food and Drug Administration (FDA) is charged with implementing the law.

Health informatics

medical informaticsBiomedical Informaticsnursing informatics
Informatics issues in data formats for sharing results (plain CSV files, FDA endorsed formats, such as CDISC Study Data Tabulation Model) are important challenges within the field of clinical research informatics.

List of federal agencies in the United States

federal agenciesfederal agencyfederal agencies of the United States
The Food and Drug Administration (FDA or USFDA) is a federal agency of the United States Department of Health and Human Services, one of the United States federal executive departments.

Center for Tobacco Products

The Center for Tobacco Products (CTP) was established by the United States Food and Drug Administration as a result of the Family Smoking Prevention and Tobacco Control Act signed by President Obama in June 2009.