
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 …
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 …
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.
Contact FDA | FDA
Aug 6, 2025 · Contact FDA Get answers to your questions and report problems with FDA-regulated products.
Warning Letters | FDA
To obtain additional available information, contact FDA. Requests to FDA for agency records should be sent to: Food and Drug Administration Division of Freedom of Information (HFI-35), …
Vaccines, Blood & Biologics | FDA
CBER is the FDA center responsible for regulating biological products for human use, ensuring their safety, effectiveness, and availability.
FDA Newsroom | FDA
The latest news and events at the U.S. Food and Drug Administration (FDA) and resources for journalists.
Pharmaceutical Inspections and Compliance | FDA
Dec 5, 2024 · FDA monitors drugs on the market to help assure they meet FDA requirements for safety and quality regardless of whether they are an application drug.
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 …