Navigate the Drugs Section

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Emergency Preparedness

Bioterrorism, drug preparedness and natural disaster response

Drug Approvals and Databases

Drug-Related Databases from FDA; Information on Drug Approvals

Drug Safety and Availability

Medication Guides, Drug Shortages, Drug Safety Communications and Other Safety Announcements

Development & Approval Process (Drugs)

Conducting Clinical Trials, Types of Drug Applications, Forms and Submissions Requirements, Labeling Initiatives, Drug and Biologic Approval Reports

Guidance, Compliance & Regulatory Information

Guidance for Industry, Warning Letters, Postmarket Surveillance Programs, Rules and Regulations

News & Events

What's New on This Site, Drug Approval Listing, Meetings and Conferences

Science & Research (Drugs)

Research by FDA Staff to Evaluate and Enhance the Safety of Drug Products

Resources for You

For Consumers, Health Professionals, Industry

Organization Profile Overview

The Food and Drug Administration (FDA or USFDA) is a federal agency of the United States Department of Health and Human Services, one of the United States federal executive departments. The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusions, medical devices, etc

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