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  1. 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 …

  2. Drugs | FDA

    FDA uses science and data to ensure that approved drugs are of a high quality, safe, and effective. Learn more about the FDA’s role in reviewing, approving, and monitoring drugs in …

  3. Recalls, Market Withdrawals, & Safety Alerts | FDA

    Recalls, Market Withdrawals, & Safety Alerts The list below provides information gathered from press releases and other public notices about certain recalls of FDA-regulated products.

  4. Regulatory Information | FDA

    Search for FDA guidance documents, learn about the laws enforced by FDA, and more.

  5. Contact FDA | FDA

    Aug 6, 2025 · Contact FDA Get answers to your questions and report problems with FDA-regulated products.

  6. Warning Letters | FDA

    To obtain additional available information, contact FDA. Requests to FDA for agency records should be sent to: Food and Drug Administration Division of Freedom of Information (HFI-35), …

  7. Vaccines, Blood & Biologics | FDA

    CBER is the FDA center responsible for regulating biological products for human use, ensuring their safety, effectiveness, and availability.

  8. FDA Newsroom | FDA

    The latest news and events at the U.S. Food and Drug Administration (FDA) and resources for journalists.

  9. Pharmaceutical Inspections and Compliance | FDA

    Dec 5, 2024 · FDA monitors drugs on the market to help assure they meet FDA requirements for safety and quality regardless of whether they are an application drug.

  10. FDA Dashboards - Inspections

    FDA does not issue CGMP certificates at the conclusion of an inspection. Instead, this dashboard provides the outcomes, including classification and other details, of a firm’s most recent …