- 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
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
- About FDA | FDA - U. S. Food and Drug Administration
General information about FDA – its mission, history, organization, partnerships, etc
- FDA Newsroom | FDA
The latest news and events at the U S Food and Drug Administration (FDA) and resources for journalists
- 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
- 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
- Inspection Classification Database | FDA
The Food and Drug Administration (FDA) inspects and assesses regulated facilities to determine a firm's compliance with applicable laws and regulations, such as the Food, Drug, and Cosmetic Act
- Laws Enforced by FDA
Among other provisions, the law authorized the FDA to demand evidence of safety for new drugs, issue standards for food, and conduct factory inspections
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