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 - U.S. Food and Drug Administration
The Center for Drug Evaluation and Research (CDER) ensures that safe and effective drugs are available to improve the health of the people in the United States
What We Do | FDA - U.S. Food and Drug Administration
The Food and Drug Administration is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical ...
Medical Devices | FDA - U.S. Food and Drug Administration
FDA regulates the sale of medical device products in the U.S. and monitors the safety of all regulated medical products.
Contact FDA | FDA - U.S. Food and Drug Administration
2024年10月21日 · Contact information for the U.S. Food and Drug Administration.
FDA en español | FDA - U.S. Food and Drug Administration
Página principal en español de la Administración de Alimentos y Medicamentos de los Estados Unidos (FDA)
Recalls, Market Withdrawals, & Safety Alerts | FDA
2024年10月1日 · Date Brand Name(s) Product Description Product Type Recall Reason Description Company Name Terminated Recall Excerpt; 01/24/2025: Provepharm Inc. Phenylephrine hydrochloride Injection, USP, 10 mg/ mL
¿Qué regula la FDA? | FDA - U.S. Food and Drug Administration
La FDA regula una amplia gama de productos médicos, veterinarios, biológicos, de tabaco y alimentos, excepto la mayoría de los productos de carne y avícolas, que están regulados por el ...
FDA en español | FDA
La FDA es responsable de proteger la salud pública asegurando la seguridad, eficacia y protección de los medicamentos, los productos biológicos y los dispositivos médicos humanos y ...
FDAAA Certification to Accompany Drug, Biological Product
The recently enacted U.S. Public Law 110-85 (Food and Drug Administration Amendments Act of 2007), Title VIII, Section 801 mandates the expansion of the clinical trials data bank (ClinicalTrials ...
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