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  2. Emergency Use Authorization - Wikipedia

    en.wikipedia.org/wiki/Emergency_Use_Authorization

    An Emergency Use Authorization (EUA) in the United States is an authorization granted to the Food and Drug Administration (FDA) under sections of the Federal Food, Drug, and Cosmetic Act as added to and amended by various Acts of Congress, including by the Pandemic and All-Hazards Preparedness Reauthorization Act of 2013 (PAHPRA), as codified by 21 U.S.C. § 360bbb-3, to allow the use of a ...

  3. Report: FDA lags on food safety inspections due to COVID-19 ...

    www.aol.com/news/report-fda-lags-food-safety...

    (The Center Square) – Facing personnel shortages and pandemic disruptions, the U.S. Food and Drug Administration has failed to meet requirements for food safety inspections since 2018, according ...

  4. Food and Drug Administration - Wikipedia

    en.wikipedia.org/wiki/Food_and_Drug_Administration

    The United States Food and Drug Administration (FDA or US FDA) is a federal agency of the Department of Health and Human Services.The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, tobacco products, caffeine products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines ...

  5. Pandemic and All-Hazards Preparedness Reauthorization Act of ...

    en.wikipedia.org/wiki/Pandemic_and_All-Hazards...

    (5) authorize FDA to waive a product's Risk Evaluation and Mitigation Strategy if necessary. Section 303 contains official definitions for security countermeasure, qualified countermeasure and qualified pandemic or epidemic product that will be added to the Federal Food, Drug and Cosmetic Act. [4]

  6. Hundreds of FDA staff return to work amid shutdown ... - AOL

    www.aol.com/news/hundreds-fda-staff-return-amid...

    The FDA employees returning to work, mostly without pay, include about 100 staff focused on inspections of high-risk medical device manufacturing facilities, about 70 focused on inspections of ...

  7. Criticism of the Food and Drug Administration - Wikipedia

    en.wikipedia.org/wiki/Criticism_of_the_Food_and...

    Numerous governmental and non-governmental organizations have criticized the U. S. Food and Drug Administration for alleged excessive and/or insufficient regulation.The U.S. Food and Drug Administration (FDA) is an agency of the United States Department of Health and Human Services and is responsible for the safety regulation of most types of foods, dietary supplements, drugs, vaccines ...

  8. US FDA clears use of Cresilon's gel to stop severe bleeding ...

    www.aol.com/news/us-fda-clears-cresilons-gel...

    The U.S. Food and Drug Administration has cleared Cresilon's gel to quickly control bleeding, the privately held company said on Thursday, potentially giving emergency medical technicians and ...

  9. List of COVID-19 pandemic legislation - Wikipedia

    en.wikipedia.org/wiki/List_of_COVID-19_pandemic...

    Coronavirus Preparedness and Response Supplemental Appropriations Act, 2020 – March 2020; Families First Coronavirus Response Act – March 2020; Coronavirus Aid, Relief, and Economic Security Act (CARES Act) – Includes $1200 stimulus checks, March 2020