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The U.S. Food and Drug Administration (FDA) is a federal agency of the Department of Health and Human Services. 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 safety of our nation's food supply, cosmetics, and products that emit radiation. The FDA also has responsibility for regulating the manufacturing, marketing, and distribution of tobacco products to protect the public health and to reduce tobacco use by minors. Its work is critical to improving health outcomes and safeguarding citizens from harmful products.
Serves as the central hub for the agency's regulatory activities, policy development, research, and administrative operations, overseeing the safety and efficacy of a wide range of products.
The White Oak campus is a large, modern facility featuring state-of-the-art laboratories, extensive office buildings, conference facilities, a library, and a visitor center. It was designed to foster collaboration and scientific innovation.
The work culture at the FDA headquarters is mission-driven, characterized by a strong commitment to public health and safety. It involves a blend of scientific rigor, regulatory diligence, and public service, with collaboration among scientists, doctors, policy analysts, and administrative staff.
The White Oak campus is significant as it centralizes FDA operations, allowing for improved efficiency, communication, and collaboration across its various centers and offices, crucial for its complex regulatory mission.
While primarily a U.S. domestic agency, the FDA has a significant global impact and presence. It operates international offices in key regions such as China, India, Europe, and Latin America. These offices facilitate inspections of foreign manufacturing sites, engage with foreign regulatory authorities, enhance cooperation on product safety and quality, and help ensure that imported products meet U.S. standards. The FDA also participates in international forums and partnerships to harmonize regulatory approaches and address global health challenges.
10903 New Hampshire Ave
Silver Spring
MD
USA
Address: 3900 NCTR Road, Jefferson, AR 72079
Serves as a major research hub, providing scientific data and expertise on the toxicity of regulated products, which informs regulatory decisions nationwide.
Address: Multiple field offices and laboratories nationwide (e.g., ORA - Office of Regulatory Affairs field offices).
To ensure compliance with federal regulations at the local and regional levels, inspect manufacturing facilities, oversee imported products, and respond to public health emergencies.
Address: International posts in regions like China, India, Europe, and Latin America.
To ensure the safety and quality of imported products and to foster international cooperation on health and regulatory standards.
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As of April 2025, Food and Drug Administration' leadership includes:
Food and Drug Administration has been backed by several prominent investors over the years, including:
High-level appointments and departures at the FDA are significant events, often involving Senate confirmations for roles like the Commissioner. Center Directors and Deputy Commissioners are also key leadership positions. Tracking is based on official announcements.
Discover the tools Food and Drug Administration uses. Highperformr reveals the technologies powering your target accounts — helping your sales, marketing, and GTM teams prioritize smarter and close faster.
The Food and Drug Administration (FDA), as a U.S. government agency, typically uses email addresses ending with the '@fda.hhs.gov' domain. The most common format is 'firstname.lastname@fda.hhs.gov'.
firstname.lastname@fda.hhs.gov
Format
john.doe@fda.hhs.gov
Example
90%
Success rate
FDA.gov • April 9, 2024
The FDA provided its weekly roundup of agency news, including updates on approvals, recalls, safety alerts, and other regulatory actions and public health information....more
FDA.gov • April 5, 2024
The FDA announced a proposed rule to amend the agency’s regulations to make explicit that laboratory developed tests (LDTs) are devices under the Federal Food, Drug, and Cosmetic Act....more
FDA.gov • February 27, 2024
The FDA outlined recent and ongoing efforts to enhance the regulation and oversight of dietary supplements to better protect consumers, including increased enforcement and calls for modernizing the regulatory framework....more
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