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14 Apr 2014, 6:30 am
Under this theory, Judge Pryor is really responding to the long string of decisions by the Obama administration to decline to follow or enforce the law. [read post]
15 Dec 2018, 9:00 am by Michael H Cohen
“New dietary ingredients” (i.e., dietary ingredients that were not marketed in the United States in a dietary supplement before October 15, 1994) will require a New Dietary Ingredient (NDI) submission to FDA. [read post]
28 Jan 2022, 7:01 am by Steven Arrigg Koh
In a new article, “The Criminalization of Foreign Relations,” I take up such questions, arguing that the United States best harnesses extraterritorial law enforcement policy when engaging criminal justice’s distinctiveness and expressivism. [read post]
24 May 2022, 11:39 am by Katherine Pompilio
  Active shooter incidents in the United States increased by more than 50 percent in 2021, writes the Hill. [read post]
29 Apr 2015, 11:15 am
This complaint asserts patent infringement arising out of the filing by Lupin of an Abbreviated New Drug Applications ("ANDA") with the United States Food and Drug Administration ("FDA") seeking approval to manufacture and sell generic versions of two pharmaceutical products - Effient 5mg and Effient 10mg tablets - prior to the expiration of the '703 patent and the '325 patent. [read post]
3 Apr 2020, 1:45 am by Frantzeska Papadopoulou
But orphan drug status is also awarded in the US if the disease affects more than 200,000 people when “there is no reasonable expectation that costs of research and development of the drug for the indication can be recovered by sales of the drug in the United States”. [read post]
18 Dec 2017, 11:57 am by Alex Potcovaru
The drug scheme included the shipment of cocaine to the United States. [read post]
24 Oct 2014, 10:41 am by Ryan Scoville
If it wanted to, the Administration could return the United States to compliance by enforcing existing laws that are valid under this precedent. [read post]
“Specialty drugs” are a fast growing sector of the pharmaceutical industry and are predicated to represent 50 percent of drug expenditures in the United States by 2020.[1] Specialty drugs are typically dispensed by specialty pharmacies. [read post]
3 Sep 2013, 3:46 pm by Betsy McKenzie
And, more disturbing to U.S. citizens, Drug Enforcement Administration (DEA) agents appear to have had access for six years to a database of telephone calls that dwarfs that used by the NSA. [read post]
28 Mar 2012, 8:30 am by Steve Hall
The Obama administration argued the FDA had discretion to allow unapproved drugs into the United States. [read post]
27 Nov 2013, 6:00 am
Food and Drug Administration ("FDA") for approval to market a generic version of Lilly's Axiron product. [read post]
18 May 2020, 4:47 pm by Moll Law Group
Earlier this month, the Food and Drug Administration (FDA) issued a warning regarding Photo Credit:g0d4ather/Shutterstock.com two breast implant manufacturers for their failure to comply with specific regulatory requirements. [read post]
30 Mar 2011, 9:14 am by Steve Hall
In addition, Soucie said he can find no evidence that Kayem or Neon Laboratories are registered with the Drug Enforcement Administration and authorized to deliver controlled substances to the United States. [read post]
9 Dec 2015, 5:16 am
  The District Court Judge then pointed out that the Government complied with the Court's order by providing a declaration from Robert Patterson, an Assistant Special Agent in Charge at the United States Drug Enforcement Administration (`DEA’), which the Government initially filed ex parte and under seal and later filed publicly in redacted form. [read post]
12 Nov 2013, 1:10 pm by Cyrus Farivar
Specifically, the FOIA request applies to a number of federal agencies, including the United States Department of Justice, the FBI, the Drug Enforcement Administration, the Office of Legal Counsel, and the executive offices of a number of United States Attorneys, including those in California, Massachusetts, Texas, and other places. [read post]
12 Sep 2023, 1:35 pm by Delia A. Deschaine
In a letter dated August 29, 2023, Rachel Levine (HHS Assistant Secretary for Health), provided a formal recommendation to Anne Milgrim (Agency Administrator) at the United States Drug Enforcement Agency (DEA) to reclassify cannabis from a Schedule I drug to a Schedule III drug under the Federal Controlled Substances Act (CSA). [read post]