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4 Nov 2010, 9:00 am by Lucas A. Ferrara, Esq.
The Food and Drug Administration (FDA) and more than 3,000 state, local, territorial, and tribal agencies work cooperatively to help keep retail food safe throughout the United States. [read post]
20 Jan 2012, 1:59 am
Food and Drug Administration, and, not surprisingly, the agency is already behind on some major deadlines in its efforts to implement it. [read post]
21 Jul 2011, 2:59 am
Food and Drug Administration (FDA) officials have been having lately with parties outside the agency are said to be about implementing and funding the new Food Safety Modernization Act.But on June 30, when Michael R. [read post]
17 Sep 2009, 1:00 pm
Portex Pediatric Tracheal Tubes were urgently recalled by the U.S Food & Drug Administration and their manufacturer Smiths Medical on September 11, 2009. [read post]
5 Feb 2009, 8:28 am
Food and Drug Administration, Center for Food Safety and Applied Nutrition Rockville, MD Rear Admiral Ali S. [read post]
15 Jan 2013, 12:58 pm by Dr. Robert Lawrence
Smith of the Johns Hopkins Center for a Livable Future. [read post]
19 Jun 2017, 11:15 am by Edward Smith
New Amputation Safety Warning Label for Diabetes Drug Invokana I’m Ed Smith, a Sacramento personal injury lawyer. [read post]
9 Mar 2010, 11:14 am
In a recent crackdown on false and misleading claims on food packages, the Food and Drug Administration has sent warning letters to 17 producers for making what it alleges are misleading statements about nutrition and health benefits. [read post]
13 Mar 2011, 6:39 am by M. Brandon Smith
Food and Drug Administration (FDA), has issued a voluntary recall of four lots of Whey-26 Protein Powder due to possible Salmonella contamination. [read post]
12 Apr 2010, 7:15 pm by Drew Falkenstein
  The bill substantially modifies the Federal Food Drug and Cosmetics Act, and generally gives the Food and Drug Administration better authority and ability to monitor the safety of our food supply, and take quicker and more effective action for food companies that don't adequately protect against foodpoisoning risks. [read post]
28 Apr 2024, 7:32 pm by Elliott Race
Prior drug exclusion at issue The primary barrier facing the FDA is the application of the drug exclusions in Sections 301(II) and 201(ff) of the Federal Food, Drug and Cosmetic Act (FD&C Act), which the FDA has concluded apply to CBD. [read post]
10 Jul 2014, 7:29 pm by CSSFIRM.COM
Food and Drug Administration (FDA) approved Xarelto in July 2011 to reduce the risk of blood clots, deep vein thrombosis (DVT) and pulmonary embolism (PE) in patients with a history of knee or hip replacement surgery. [read post]
20 Jun 2013, 12:14 am by Helena Bottemiller
Food and Drug Administration and the Center for Food Safety have not been able to come to an agreement on a proposed schedule of Food Safety Modernization Act (FSMA) deadlines despite a court order to do so by May 20. [read post]
13 Jul 2010, 9:38 am
In a July 12, 2010 article by Gardiner Harris in the New York Times, it was revealed that since Avandia's success was so vital to SmithKline, company executives decided not to publicize results of studies on its website or, more importantly, to submit these negative results to drug regulators at the Food & Drug Administration. [read post]
5 May 2011, 2:59 am
"The industry wants the FDA to turn a blind eye to evidence of misuse of drugs on dairy farms," said Caroline Smith DeWaal, food safety director of CSPI. [read post]
3 Sep 2007, 8:08 pm
At Justice, he defended the constitutionality of a number of federal statutes, including the Family and Medical Leave Act and the Food and Drug Modernization Act, in cases that, ultimately, were resolved by the Supreme Court. [read post]
15 Dec 2020, 9:53 am by Dennis Crouch
Novartis Pharmaceuticals Corporation (Supreme Court 2020) Introducing generic alternatives that compete with previously approved drugs requires market approval through the Food and Drug Administration (“FDA”). [read post]