U.S. Food and Drug Administration
The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the ...
Drugs | FDA
FDA uses science and data to ensure that approved drugs are of a high quality, safe, and effective. Learn more about the FDA’s role in reviewing, approving, and monitoring drugs in the latest ...
Recalls, Market Withdrawals, & Safety Alerts | FDA
Recalls, Market Withdrawals, & Safety Alerts The list below provides information gathered from press releases and other public notices about certain recalls of FDA-regulated products.
Regulatory Information | FDA
Search for FDA guidance documents, learn about the laws enforced by FDA, and more.
Medical Devices | FDA
FDA regulates the sale of medical device products in the U.S. and monitors the safety of all regulated medical products.
Food | FDA
Food Code 2022 Commemorating 30-years of the FDA Food Code - a model for best practices to ensure the safe handling of food in a retail setting
Drug Approvals and Databases | FDA
Sep 24, 2025 · Novel Drugs at FDA: CDER’s New Molecular Entities and New Therapeutic Biological Products Drug and Biologic Approval and IND Activity Reports This Week's Drug Approvals Drug …
Press Announcements | FDA
Note: Press announcements from 2004-2012, 2013-2016, 2017, 2018-2020, 2021, 2022, and 2023 are available through the FDA.gov Archive. Some links in press announcements may no longer be active.
FDA Newsroom | FDA
The latest news and events at the U.S. Food and Drug Administration (FDA) and resources for journalists.
FDA Dashboards - Inspections
FDA does not issue CGMP certificates at the conclusion of an inspection. Instead, this dashboard provides the outcomes, including classification and other details, of a firm’s most recent inspection.