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The US Supreme Court Wednesday released an order temporarily extending access to the abortion pill mifepristone, giving the court more time to consider the suspension of the Food and Drug Administration’s (FDA) approval of the drug over 20 years ago. [read post]
28 Sep 2019, 3:52 pm by Tom Smith
Drugs that are being used to halt puberty in gender-confused youth have been linked to thousands of adult deaths, government data show.The Food & Drug Administration has recorded thousands of deaths associated with Lupron, a puberty-blocking drug that is routinely used to treat prostate cancer in men and endometriosis in women. [read post]
Food and Drug Administration announces new partnership with Canadian Food Inspection Agency on food safety appeared first on Health Law Pulse. [read post]
US Supreme Court Justice Samuel Alito Friday issued an order extending a temporary block on a lower Texas federal judge’s decision to suspend the US Food and Drug Administration’s (FDA) approval of the abortion drug mifepristone. [read post]
31 May 2022, 9:00 pm by News Desk
The Food and Drug Administration is continuing its use of import alerts to enforce U.S. food safety regulations for food from foreign countries. [read post]
13 Jun 2017, 7:57 am by Robert Kraft
In a 1,311-word article, Bloomberg News reports that last year the US Food and Drug Administration faced a dilemma of “whether to allow importation of drug ingredients from a Chinese factory with a history of poor quality controls, or face shortages of treatments for American cancer patients. [read post]
10 Nov 2015, 7:53 am by Robert Kraft
Modern Healthcare reports that the Food and Drug Administration announced a new rule that drugs entering the US will be destroyed if they “are found to have been ‘adulterated, misbranded or unapproved’ and in violation of the Food, Drug and Cosmetic Act” because the medicines would pose a health risk. [read post]
Food and Drug Administration (“FDA”) regarding its commitments set forth under the Prescription Drug Under Fee Act Reauthorization Performance Goals and Clinical Trial Diversity and Modernization mandates established by Congress under the Food and Drug Omnibus Reform Act of 2022 (FDORA), including developments on the intersection and use of digital health technology in clinical trials and clinical trial diversity. [read post]
16 Sep 2011, 1:30 am
A US Food and Drug Administration advisory panel has said that there isn't enough information available for it to recommend limits for how long a patient should take a bisphosphonate drug to treat osteoporosis. [read post]
2 Nov 2011, 8:47 am
The US Food and Drug Administration (FDA) has begun a nationwide effort to test pet food for salmonella contamination.FDA investigators have started taking samples of dry pet food, pet treats and diet supplements from distributors, wholesales and retailers such as PetSmart, Petco, Walmart, Costco, and Target. [read post]
4 Dec 2018, 1:44 am by Kluwer Patent blogger
Kluwer Patent bloggerThe American Food Drug Administration (FDA) will follow the European Medicines Agency from London to Amsterdam because of the Brexit. [read post]
16 Sep 2014, 7:02 am by Pete Strom
Indian Company Under Fire Again for Warfarin Drug Recall Sun Pharmaceuticals has been closely scrutinized by the Food and Drug Administration recently for problems with generic drugs leading to drug recalls in the US. [read post]
17 Aug 2020, 10:00 pm
Morgan Lewis partner Robert Hibbert and associate Maria Kalousi-Tatum authored a Food Safety Magazine article about the US Food and Drug Administration (FDA) and the US Department of Agriculture’s memorandum of understanding (MOU) intended to prevent potential disruptions to the food supply chain resulting from the COVID-19 pandemic. [read post]
17 Aug 2020, 10:00 pm
Morgan Lewis partner Robert Hibbert and associate Maria Kalousi-Tatum authored a Food Safety Magazine article about the US Food and Drug Administration (FDA) and the US Department of Agriculture’s memorandum of understanding (MOU) intended to prevent potential disruptions to the food supply chain resulting from the COVID-19 pandemic. [read post]
17 Aug 2020, 10:00 pm
Morgan Lewis partner Robert Hibbert and associate Maria Kalousi-Tatum authored a Food Safety Magazine article about the US Food and Drug Administration (FDA) and the US Department of Agriculture’s memorandum of understanding (MOU) intended to prevent potential disruptions to the food supply chain resulting from the COVID-19 pandemic. [read post]
17 Aug 2020, 10:00 pm
Morgan Lewis partner Robert Hibbert and associate Maria Kalousi-Tatum authored a Food Safety Magazine article about the US Food and Drug Administration (FDA) and the US Department of Agriculture’s memorandum of understanding (MOU) intended to prevent potential disruptions to the food supply chain resulting from the COVID-19 pandemic. [read post]
17 Aug 2020, 10:00 pm
Morgan Lewis partner Robert Hibbert and associate Maria Kalousi-Tatum authored a Food Safety Magazine article about the US Food and Drug Administration (FDA) and the US Department of Agriculture’s memorandum of understanding (MOU) intended to prevent potential disruptions to the food supply chain resulting from the COVID-19 pandemic. [read post]
17 Aug 2020, 10:00 pm
Morgan Lewis partner Robert Hibbert and associate Maria Kalousi-Tatum authored a Food Safety Magazine article about the US Food and Drug Administration (FDA) and the US Department of Agriculture’s memorandum of understanding (MOU) intended to prevent potential disruptions to the food supply chain resulting from the COVID-19 pandemic. [read post]
20 Jun 2011, 3:28 pm by info@thomasjhenrylaw.com
The Food and Drug Administration conducted a three-part study which examined the usefulness of print advertisements for prescription drugs. [read post]