- 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
- 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
- About FDA | FDA - U. S. Food and Drug Administration
General information about FDA – its mission, history, organization, partnerships, etc
- Drug Safety and Availability | FDA
Advances in FDA's Drug Safety Programs (annual reports) Index to Drug-Specific Information FDA Drug Safety Podcasts FDA’s Labeling Resources for Human Prescription Drugs MedWatch Statement on
- Novel Drug Approvals for 2025 | FDA
To see the FDA-approved conditions of use [e g , indication (s), population (s), dosing regimen (s)] for each of these products, please see the most recently approved Prescribing Information (or
- Forms | FDA
Listing of all external Forms both OMB approved and state using ORA forms
- 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
- Outbreak Investigation of Listeria monocytogenes: Ready-to-Eat Foods . . .
The FDA and CDC, in collaboration with state and local partners, are investigating illnesses in a multistate outbreak of Listeria monocytogenes infections linked to Ready-to-Eat (RTE) foods, or
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