Search for: "Unite Here v. Food and Drug Administration" Results 81 - 100 of 444
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31 Dec 2007, 1:36 pm
Commissioner of Food and Drugs, 740 F.2d at 34. [read post]
28 Dec 2006, 5:32 pm
Court ofAppeals1996-2001 Private practice, Washington, D.C.2001-2003 Associate Chief Counsel, Food & Drug Administration Rockville, MD2004 Law clerk, chambers of the Honorable Elizabeth McClanahan, Court ofAppeals of Virginia, Abingdon2005-2006 Private practice in Abingdon, Virginia [read post]
2 Jan 2018, 5:00 am by Paul Rosenzweig
  Regulatory agencies like the Food and Drug Administration and the National Highway Traffic Safety Administration will use existing authorities to impose security and privacy requirements on consumer goods – hopefully in the form of standards but possibly in the form of mandates. [read post]
24 Oct 2013, 10:12 am by Mark Zamora
Food and Drug Administration, 4040 North Central Expressway, Suite 300, Dallas, Texas 75204. [read post]
22 Apr 2014, 7:41 am
  Procedural HistoryThe New Drug Application (NDA) for the Tarka® product was approved by the Food and Drug Administration in 1996 and acquired by Abbott Laboratories in 2001. [read post]
3 Sep 2013, 9:01 am by Mary Dwyer
Stengel 12-1351Issue: Whether the Medical Device Amendments to the federal Food, Drug, and Cosmetic Act preempt a state-law claim alleging that a medical device manufacturer violated a duty under federal law to report adverse-event information to the Food and Drug Administration. [read post]
17 May 2018, 1:06 pm by Blake Marcus
Coupled with the United States Supreme Court’s decision in Illinois v. [read post]
3 Nov 2008, 5:00 am
Wyeth countered that because use of the warning label was mandated by the FDA pursuant to its authority under the Food, Drug and Cosmetic Act (FDCA), Ms. [read post]
10 Feb 2012, 8:39 am by Bexis
  The would-be class consisted of:all other persons similarly situated, throughout the United States, who are domociled [sic] in one of the fifty states, including Ohio, and who are consumers who received ANY vaccine or drug with a PharmaJet injector device where the specific vaccine or specific drug does not have the stated approval by the FDA for administration with a “needleless injector” or “needle-free injector,” also know [sic]… [read post]
4 Apr 2012, 1:41 pm by John J. Sullivan
  The FDA’s powers come from the Federal Food, Drug & Cosmetics Act (“FDCA”). [read post]
The Supreme Court has construed the safe harbor to apply to drugs as well as medical devices and other products subject to Food and Drug Administration (FDA) approval. [read post]
The Supreme Court has construed the safe harbor to apply to drugs as well as medical devices and other products subject to Food and Drug Administration (FDA) approval. [read post]
The Supreme Court has construed the safe harbor to apply to drugs as well as medical devices and other products subject to Food and Drug Administration (FDA) approval. [read post]
7 Jul 2015, 1:55 pm
Food and Drug Administration for approval to market a generic version of Lilly's Axiron product constitutes patent infringement. [read post]