FDA

FDA

Government Administration

Silver Spring, MD 730,622 followers

About us

The Food and Drug Administration is an agency within 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. 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. FDA is responsible for advancing the public health by helping to speed innovations that make medical products more effective, safer, and more affordable and by helping the public get the accurate, science-based information they need to use medical products and foods to maintain and improve their health. FDA also plays a significant role in the Nation's counterterrorism capability. FDA fulfills this responsibility by ensuring the security of the food supply and by fostering development of medical products to respond to deliberate and naturally emerging public health threats.

Website
http://www.fda.gov/
Industry
Government Administration
Company size
10,001+ employees
Headquarters
Silver Spring, MD
Type
Government Agency
Specialties
Food, Drugs, Medical Devices, Vaccines Blood and Biologics, Animal and Veterinary, Cosmetics, Radiation-Emitting Products, Tobacco Products, Regulatory Research, and Toxicological Regulatory Research

Locations

Employees at FDA

Updates

  • View organization page for FDA, graphic

    730,622 followers

    Test your knowledge in anticipation of our upcoming webinar, “FDA Drug Topics: Fraudulent Products: You’re Using What?” on May 21, 2024, 1:00 PM – 2:00 PM ET by responding to the question below. The answer will be posted once the poll closes. Register to attend the webinar here ➡️ https://lnkd.in/d_UedpMa

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    730,622 followers

    Are you a researcher, sponsor, or industry professional involved in bioanalysis? Do you submit INDs, NDAs, BLAs, or ANDAs that include bioanalytical study data? Are you are involved in GLP-regulated nonclinical laboratory studies and Animal Rule studies data? Then don’t miss this special, informative event. FDA experts will discuss: Expectations during BA/BE Inspections, good Laboratory Practice (GLP) /Animal Rule (AR) Compliance Programs and inspections, and more! 

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    X-ray imaging has led to improvements in the diagnosis and treatment of numerous medical conditions in pediatric patients. Health care providers are encouraged to talk with parents to ensure they have a clear understanding of benefits and risks associated with pediatric X-rays. The FDA offers information for health care professionals about X-ray imaging for children. Learn more: https://lnkd.in/guQK8cFw #HospitalWeek

    • A doctor examines X-rays of a child’s arm as the injured patient sits in the background.
  • View organization page for FDA, graphic

    730,622 followers

    As we close out this year’s #HurricanePrep Week, we want to highlight how important is to have access to #MedicalDevices during #HurricaneSeason which ultimately can save lives. The FDA encourages health care providers, device manufacturers, and distributors to take action today to minimize disruptions to patient care. Preparedness tip: Assess the risks that these events can have on your supply chain, business operations, and facilities. https://lnkd.in/ebftEe2M

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  • View organization page for FDA, graphic

    730,622 followers

    The first step of preparing for a hurricane is to know your risk. It’s #HurricanePrep Week and FDA reminds you that there’s no better time to create an emergency plan than BEFORE hurricane season. Having a disaster preparedness checklist will be very useful during hurricane season. Preparedness tip: Include important details about everyone’s #MedicalDevices and make sure they are working properly. Visit us for more #HurricaneSeason tips. https://lnkd.in/e4ZWENmm

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  • View organization page for FDA, graphic

    730,622 followers

    Do you work on over-the-counter (OTC) monograph drug products and/or non-prescription drugs? If so, attend this no-cost webinar for an overview of the Over-the-Counter Drug User Fee Program (OMUFA). Learn about fees, registration, timelines and more from FDA experts. 🔔 Don’t miss it: https://lnkd.in/dafKebhU

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  • View organization page for FDA, graphic

    730,622 followers

    Today, we issued the final guidance titled Remanufacturing of Medical Devices and announced an upcoming webinar as part of our ongoing efforts to help distinguish between #MedicalDevice remanufacturing and servicing. We issued this final guidance to help clarify the activities that are likely “remanufacturing” a medical device: https://lnkd.in/dYC2GU4 For stakeholders interested in learning more, please join us on 6/27/24 for our webinar on the final guidance: https://lnkd.in/eXjUQN6r

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