- 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
- 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
- At-Home OTC COVID-19 Diagnostic Tests | FDA
The table below is updated regularly and lists FDA-authorized at-home OTC COVID-19 diagnostic tests, who can use the test, links to home use instructions for each test, and other details that may
- Warning Letters | FDA
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
- FDA Industry Systems
FDA Industry Systems (FIS) was created to facilitate making submissions to the U S Food and Drug Administration (FDA), including registrations, listings, and other notifications FIS has been available 24 hours a day, seven days a week, since October 16, 2003 6:00 p m EDT
- 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
- Establishment Registration Device Listing
Note: Registration of a device establishment, assignment of a registration number, or listing of a medical device does not in any way denote approval of the establishment or its products by FDA
- What We Do | FDA
FDA fulfills this responsibility by ensuring the security of the food supply and by fostering development of medical products to respond to deliberate and naturally emerging public health threats
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