Search for: "UNITED STATES FOOD & DRUG ADMINISTRATION "
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3 Nov 2022, 9:05 pm
Food and Drug Administration (FDA) announced efforts to increase the availability of infant formula in the United States by permitting the importation of formula products from Ireland and New Zealand. [read post]
24 Nov 2021, 6:17 am
On July 14, 2021, the United States Food and Drug Administration (FDA) announced Johnson & Johnson’s voluntary recall of all lots of the following sunscreen products: Neutrogena Beach Defense aerosol sunscreen; Neutrogena Cool Dry Sport aerosol sunscreen; Neutrogena Invisible Daily Defense aerosol sunscreen; Neutrogena Ultra Sheer aerosol sunscreen; and Aveeno Protect + Refresh aerosol sunscreen. [read post]
24 Dec 2011, 9:44 am
The United States does not have an orthopedic registry, and the Food and Drug Administration is researching to see whether data from sources like overseas databases and registries run by hospitals here can be used to better monitor device performance. [read post]
24 Nov 2021, 6:17 am
On July 14, 2021, the United States Food and Drug Administration (FDA) announced Johnson & Johnson’s voluntary recall of all lots of the following sunscreen products: Neutrogena Beach Defense aerosol sunscreen; Neutrogena Cool Dry Sport aerosol sunscreen; Neutrogena Invisible Daily Defense aerosol sunscreen; Neutrogena Ultra Sheer aerosol sunscreen; and Aveeno Protect + Refresh aerosol sunscreen. [read post]
21 Nov 2010, 9:00 am
As part of the same effort, the federal Food and Drug Administration is introducing new cigarette warning labels with graphic images depicting the health risks of smoking. [read post]
24 Nov 2021, 6:17 am
On July 14, 2021, the United States Food and Drug Administration (FDA) announced Johnson & Johnson’s voluntary recall of all lots of the following sunscreen products: Neutrogena Beach Defense aerosol sunscreen; Neutrogena Cool Dry Sport aerosol sunscreen; Neutrogena Invisible Daily Defense aerosol sunscreen; Neutrogena Ultra Sheer aerosol sunscreen; and Aveeno Protect + Refresh aerosol sunscreen. [read post]
30 Oct 2013, 9:39 pm
E-cigarettes constitute a rapidly growing $1.7 billion market, and the Food and Drug Administration (FDA) has indicated that it is planning to regulate these products. [read post]
14 Feb 2020, 12:49 pm
Kitty Block is President and CEO of the Humane Society of the United States. [read post]
8 Jun 2022, 5:23 am
Beyond these declarations, there are others available to HHS, including those under section 564 of the Food, Drug, and Cosmetic Act, which allow FDA to use Emergency Use Authorizations (EUAs) as the basis to authorize not otherwise approved drugs, devices, and other therapies. [read post]
7 Mar 2019, 9:30 pm
Food and Drug Administration (FDA), which will take effect in one month. [read post]
6 Mar 2017, 12:47 pm
However, the CDC, several state health departments and the Food and Drug Administration are warning consumers not to eat any I.M. [read post]
18 Dec 2018, 9:30 pm
Food and Drug Administration. [read post]
14 May 2015, 11:09 am
Department of Agriculture’s Food Safety and Inspection Service (FSIS) and the Food and Drug Administration that tracks incidents of Campylobacter, Listeria, Salmonella, Shigella, Shiga toxin-producing E. coli (STEC) O157, STEC non-O157, Vibrio, Yersinia, Cryptosporidium and Cyclospora. [read post]
13 Dec 2018, 1:59 pm
The statistics above are for the United States as of Dec. 13. [read post]
7 Mar 2023, 7:14 am
Additional criteria and limitations apply in the context of these proposed rules, including new and modified administrative and record-keeping requirements. [read post]
8 Sep 2020, 2:50 pm
The Food and Drug Administration has asked the justices to freeze that order and reinstate the federal requirement that the drug be picked up in person from a health care provider. [read post]
25 Oct 2018, 9:30 pm
Food and Drug Administration (FDA)—the federal agency that regulates the pharmaceutical industry. [read post]
8 Jun 2016, 5:20 am
Food & Drug Administration. [read post]
25 May 2007, 8:57 am
Earlier, the Supreme Court had asked for the government’s views on the antitrust effects of settlement agreements between holders of drug patents and generic drug makers enjoying the 180-day market exclusivity after Food and Drug Administration approval. [read post]
7 Aug 2011, 5:31 pm
Additionally, the Food and Drug Administration has not yet promulgated any regulations to implement the biosimilars provisions of the new law, nor has the Agency approved any biosimilars in the United States. . . . [read post]
