- 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
- Regulatory Information | FDA
Search for FDA guidance documents, learn about the laws enforced by FDA, and more
- 关于美国食品和药物管理局（FDA）批准和不批准的 10 个事实#FDAFacts
FDA 负责确定人类和兽用食品和药物、生物和烟草产品、医疗器械、化妆品以及放射辐射产品的安全性、有效性和保障性，以保护公众健康。
- 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 - Home
The Data Dashboard contains data elements from FDA compliance and enforcement data sources, including Inspections, Compliance Actions, Recalls, Imports, and Food Safety Modernization Act programs
- Medical Device Databases | FDA
CDRH Databases: a listing of databases for such topics as advisory committees, regulations, good practices, medical devices, Premarket Approval (PMA) and Notification (510 (k)), product codes
- Roadmap to Reducing Animal Testing in Preclinical Safety Studies
This scientific roadmap lays out an initial strategy for FDA to reduce and replace animal testing in preclinical safety assessment of drugs and biologics and will be refined based on feedback
- FDA Clears First Blood Test Used in Diagnosing Alzheimer’s Disease
The FDA, an agency within the U S Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines
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