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 - U.S. Food and Drug Administration
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
See Additional information about recalls for a more complete listing. The Recalls, Market Withdrawals & Safety Alerts are available on FDA’s website for three years before being archived.
About FDA | FDA - U.S. Food and Drug Administration
General information about FDA – its mission, history, organization, partnerships, etc.
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What We Do | FDA
FDA is responsible for advancing the public health by helping to speed innovations that make medical products more effective, safer, and more affordable and by helping the public get the accurate ...
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 …
Regulatory Information | FDA
Search for FDA guidance documents, learn about the laws enforced by FDA, and more.
Vaccines, Blood & Biologics | FDA
CBER is the FDA center responsible for regulating biological products for human use, ensuring their safety, effectiveness, and availability. CBER also educates the public to promote the safe and ...
Postmarket Drug Safety Information for Patients and Providers
Comprehensive resource page of FDA's drug safety information for patients, health care providers, and regulators.