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Food and Drug Administration

The Food and Drug Administration (FDA) is a part of the U.S. Department of Health and Human Services. The FDA is responsible for protecting public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the safety of the food supply, cosmetics, and dietary supplements. The FDA also regulates the manufacturing, marketing, and distribution of products that are aimed at treating, diagnosing, curing, or preventing diseases. The FDA website provides the public with information about the role of the FDA and its regulations, as well as links to databases and other resources related to food and drug safety.

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  • Country
    Hosted in United States

  • Traffic rank
    #383 Site Rank

  • Site Owner information
    Whois info

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Site is not blacklisted

  • Formed
    June 30, 1906

  • Headquarters
    White Oak Campus,10903,New Hampshire Avenue,Silver Spring, Maryland,20993

  • Preceding agencies
    Food, Drug, and Insecticide Administration (July 1927 to July 1930),Bureau of Chemistry,,USDA,(July 1901 through July 1927),Division of Chemistry, USDA (established 1862)

  • Jurisdiction
    Federal government of the United States

  • Employees
    18,000 (2022)

  • Annual budget
    US$6.5 billion (2022)

  • Agency executive
    Robert Califf,,,Commissioner

  • Parent agency
    Department of Health and Human Services

Traffic rank
#383
Site age
Location
United States
Popular Questions for Food and Drug Administration
What is the role of the FDA in drug approval? Answer: The FDA plays a critical role in the approval of new drugs. The agency is responsible for assessing the safety, efficacy, and quality of drugs and ensuring that they meet the required standards for approval. The FDA reviews drug applications submitted by pharmaceutical companies and holds public meetings to provide a forum for discussion of scientific issues related to the approval of new drugs. The agency also reviews clinical trial results and other scientific data to assess the safety and efficacy of new drugs. Once the FDA is satisfied that a drug meets the safety, efficacy, and quality standards, it approves the drug for sale in the United States.
What is the FDA's role in medical device safety? Answer: The FDA is responsible for ensuring the safety and effectiveness of medical devices. The agency sets standards and regulations related to the manufacturing, labeling, and distribution of medical devices. The FDA also requires companies to provide safety data on the devices and submit pre-market approval applications for certain medical devices. The agency also conducts inspections of medical device manufacturing facilities to ensure compliance with safety standards.
How can I report an issue with a drug or medical product to the FDA? Answer: The FDA encourages consumers to report any problems they have with drugs, medical products, or food products to the agency. Consumers can report issues to the FDA by calling 1-800-FDA-1088 or visiting the FDA website. Consumers can also report issues to their health care provider or to the manufacturer of the product. The FDA will review the reports and take appropriate action if necessary.
What is the FDA's role in food safety? Answer: The FDA is responsible for protecting the public health by ensuring the safety of the nation’s food supply. The agency is responsible for setting standards and regulations related to the production, processing, packaging, labeling, and distribution of food products. The FDA also conducts inspections of food-processing facilities and enforces food safety regulations. In addition, the agency monitors food-borne illness outbreaks and investigates the causes of food-borne illnesses. The FDA also works with state and local governments to ensure that food products meet safety standards.
What is the FDA's role in drug enforcement? Answer: The FDA is responsible for enforcing laws and regulations related to the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nation’s food supply, cosmetics, and products that emit radiation. The agency is responsible for conducting inspections, recall initiatives, and other activities to ensure compliance with applicable laws, regulations, and standards. The FDA also works with state and local governments to ensure that drugs, medical products, and food products meet safety standards.
Newest job postings for Food and Drug Administration
Consumer Safety officer
via USAJobs posted_at: 2 days agoschedule_type: Full-timesalary: 84,546 a year
This position is located in the Department of Health and Human Services (DHHS), Food and Drug Administration (FDA), Office of Regulatory Affairs (ORA), Office of Medical Products and Tobacco (OMPTO), Office of Pharmaceutical Quality Operations (OPQO), which coordinates domestic and foreign inspectional, quality and investigational activities across the field and at headquarters. This position is located in the Department of Health and Human Services (DHHS), Food and Drug Administration (FDA), Office of Regulatory Affairs (ORA), Office of Medical Products and Tobacco (OMPTO), Office of Pharmaceutical Quality Operations (OPQO), which coordinates domestic and foreign inspectional, quality and investigational activities across the field and at headquarters. Show more details...
Chemist
via USAJobs posted_at: 2 days agoschedule_type: Full-timesalary: 98,496 a year
This Direct-Hire position is in the Food and Drug Administration and is located in the Office of Scientific Coordination (OSC) which mission is to conduct peer-reviewed research and develop new scientific tools for the Food and Drug Administration (FDA) to improve public health.. This Direct-Hire position is in the Food and Drug Administration and is located in the Office of Scientific Coordination (OSC) which mission is to conduct peer-reviewed research and develop new scientific tools for the Food and Drug Administration (FDA) to improve public health.. Show more details...
Research Biological Scientist
via USAJobs posted_at: 3 days agoschedule_type: Full-timesalary: 94,199 a year
This position is located in the Food and Drug Administration (FDA), Center for Biologics Evaluation and Research (CBER), Office of Blood Research and Review (OBRR) which regulates blood products, related drugs, and devices; reviews retroviral diagnostic tests; develops policies on blood product standards; participates in inspections; and conducts research. This position is open to current permanent FDA employees only. This is a full-time, permanent This position is located in the Food and Drug Administration (FDA), Center for Biologics Evaluation and Research (CBER), Office of Blood Research and Review (OBRR) which regulates blood products, related drugs, and devices; reviews retroviral diagnostic tests; develops policies on blood product standards; participates in inspections; and conducts research.

This position is open to current permanent FDA employees only. This is a full-time, permanent position. Show more details...
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