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
Find information about most FDA-approved prescription, generic, and over-the-counter drug products. Drug Shortages Find information about drug shortages caused by manufacturing and quality ...
Recalls, Market Withdrawals, & Safety Alerts | FDA
On Oct. 1, 2024, the FDA began implementing a reorganization impacting many parts of the agency. We are in the process of updating FDA.gov content to reflect these changes.
Medical Devices | FDA - U.S. Food and Drug Administration
FDA regulates the sale of medical device products in the U.S. and monitors the safety of all regulated medical products.
Food | FDA
Commemorating 30-years of the FDA Food Code - a model for best practices to ensure the safe handling of food in a retail setting
What We Do | FDA - U.S. Food and Drug Administration
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 ...
Contact FDA | FDA - U.S. Food and Drug Administration
Oct 21, 2024 · View FDA’s proposed regulations and submit comments online (on Regulations.gov). How to comment on proposed regulations or submit petitions. Resolve a dispute. Contact the FDA Ombudsman
Drug Approvals and Databases | FDA
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 Trials Snapshots
Jobs and Training at FDA | FDA - U.S. Food and Drug Administration
Oct 10, 2024 · The Food and Drug Administration’s (FDA) mission is to protect and advance public health by helping to speed innovations that provide our nation with safe and effective medical products and that ...
Warning Letters | FDA - U.S. Food and Drug Administration
Matters described in FDA warning letters may have been subject to subsequent interaction between FDA and the letter recipient that may have changed the regulatory status of issues discussed in the ...