The Humanitarian Device Exemption Program provides a regulatory pathway for medical devices intended for diseases or conditions that affect small populations.| U.S. Food and Drug Administration
The Center for Tobacco Products (CTP)3 oversees the implementation of the Family Smoking Prevention and Tobacco Control Act.| U.S. Food and Drug Administration
CVM is responsible for regulating animal drugs and medicated feeds, and that food from treated animals is safe for human consumption.| 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| U.S. Food and Drug Administration
Process that evaluates the safety and effectiveness of Class III medical devices.| U.S. Food and Drug Administration
U.S. Food & Drug Administration| www.accessdata.fda.gov