
Safety | FDA
Learn about FDA's programs to monitor product safety, including recalls, safety alerts, problem reporting, and postmarket monitoring systems.
Guidance & Regulation (Food and Dietary Supplements) | FDA
Guidance and regulatory information on Food and Dietary Supplements; includes guidance for industry as well as manufacturing processes, food facility registration, HACCP, retail food …
Advisory Committees | FDA
About FDA public advisory committees, calendar of meetings, meeting materials, how to become an advisory committee member, guidance, and FAQs.
COVID-19 Vaccines for 2024-2025 | FDA
The FDA has approved and authorized for emergency use updated COVID-19 vaccines (2024-2025 formula) that include a monovalent (single) component that corresponds to the omicron …
Vaccines, Blood & Biologics | FDA
CBER protects and advances the public health by ensuring that biological products are safe and effective and available to those who need them.
Jobs and Training at FDA
Vacancies, fellowships, internships, and graduate and faculty programs; employment benefits; and ethics
Human Foods Program | FDA
The Human Foods Program (HFP) oversees all FDA activities related to food safety and nutrition, organized in a single group working under the Deputy Commissioner of Human Foods.
Registration and Listing | FDA
How to register facilities and products, and how to update registrations
At-Home OTC COVID-19 Diagnostic Tests | FDA
Sep 16, 2025 · Expiration dates and more about authorized at-home OTC COVID-19 diagnostic tests information.
Emergency Use Authorization for Vaccines Explained | FDA
FDA recognizes the gravity of the current public health emergency and the importance of facilitating availability, as soon as possible, of vaccines to prevent COVID-19 - vaccines that …
U.S. Food and Drug Administration
U.S. Food and Drug Administration
Medical Devices News and Events | FDA
Dec 30, 2024 · Medical device news-making events, videos, and meetings and conferences.
Learn About Drug and Device Approvals | FDA
FDA is speeding up the approval process for Drugs and Medical Devices. Learn how medical products are approved.
Food and Drug Administration
The Food and Drug Administration (FDA or the Agency) has determined the regulatory review period for ZURZUVAE is publishing this notice of that determination as required by law. FDA …