- 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
- 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
- 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。
- 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
- 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
- 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
- Drugs@FDA - Food and Drug Administration
Drugs@FDA includes most of the drug products approved since 1939 The majority of patient information, labels, approval letters, reviews, and other information are available for drug products approved since 1998
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