Search for: "BANKS v. FOOD AND DRUG ADMINISTRATION" Results 61 - 80 of 139
Sorted by Relevance | Sort by Date
RSS Subscribe: 20 results | 100 results
28 Sep 2023, 9:02 pm by Josephine A. Phillips
Drug Enforcement Administration issued a notice of proposed rulemaking that would classify ethylphenidate, a central nervous system stimulant, as a Schedule I substance under the Controlled Substances Act. [read post]
28 Mar 2012, 5:59 pm by Rebecca Tushnet
  We are interested in stopping deception: §5 for deceptive acts/practices, §12 for false advertising to induce purchase of foods, drugs, and devices. [read post]
2 Mar 2023, 9:05 pm by Bryn Hines
Food and Drug Administration (FDA) announced an import alert that aims to restrict the import of xylazine, an animal tranquilizer that has been found in illicit drugs such as fentanyl and heroin. [read post]
23 Apr 2012, 8:41 am by Amy Howe
  When generic drug makers want permission from the Food & Drug Administration (FDA) to sell their drugs, they can piggyback off the application filed by the brand-name drug maker as long as they are selling a drug that has essentially the same ingredients as the brand-name drug. [read post]
22 Nov 2017, 8:17 am by Nate Nead
During the past five years, numerous high-profile product recalls, mislabeling claims and other scandals have reduced consumer confidence in the dietary supplement industry, in addition to raising concerns among key regulatory agencies like the Food and Drug Administration. [read post]
3 Dec 2020, 9:05 pm by Sabrina Minhas
Food and Drug Administration (FDA) authorizes emergency use of a vaccine. [read post]
23 May 2019, 9:30 pm by Alana Bevan
Food and Drug Administration (FDA) would have declined to add a warning to the allegedly harmful drug’s label, failure-to-warn lawsuits under state law are barred due to a conflict with federal labeling regulations. [read post]
3 May 2012, 5:51 pm by FDABlog HPM
Section 113 of the Food and Drug Administration Modernization Act of 1997 amended the PHS Act to add Section 402, which directs the Secretary of Health and Human Services (“DHHS”), acting through the Director of the National Institutes of Health (“NIH”), to establish, maintain, and operate a data bank of information on clinical trials for drugs for serious or life-threatening diseases and conditions (i.e., ClinicalTrials.gov). [read post]
28 Jul 2022, 9:05 pm by Jillian Moss
Food and Drug Administration (FDA) announced that it had approved the use of a set of monkeypox vaccine doses manufactured at a plant located in Denmark. [read post]
26 Apr 2016, 7:26 am by Phyllis H. Marcus and Andrew W. Eklund
The ads also claimed that the Food and Drug Administration had endorsed tanning beds as being safe, despite the fact that tanning actually increases the risk of developing melanoma skin cancer. [read post]
6 Oct 2016, 9:30 pm by Justin Daniel
Food and Drug Administration (FDA) in the U.S. [read post]
3 May 2010, 8:03 pm by Two-Seventy-One Patent Blog
The claims are transformative as that “[t]he transformation is of the human body following administration of a drug and the various chemical and physical changes of the drug’s matabolites that enable their concentrations to be determined. [read post]
19 Mar 2022, 2:09 pm by admin
Food and Drug Administration (FDA) with respect to mutagenic impurities in medications provides an illustrative example of how theoretical and hypothetical risk assessment can be.[6] The FDA’s risk assessment approach is set out in a “Guidance” document, which like all such FDA guidances, describes itself as containing non-binding recommendations, which do not preempt alternative approaches.[7] The agency’s goal is devise a control strategy for any… [read post]
27 Mar 2018, 5:02 pm by Wolfgang Demino
The Access Loans are private loans originally financed by National City Bank ("National City") through the Access Loan Program. [read post]
27 Aug 2021, 9:03 pm by Karis Stephen
Food and Drug Administration, the Office of Intellectual Property Rights, the Federal Bureau of Investigation, U.S. [read post]
2 Jul 2020, 9:05 pm by Joshua Burd
Food and Drug Administration (FDA) issued guidance to assist the clinical development and vaccine licensing processes for the prevention of COVID-19. [read post]
26 Apr 2015, 10:07 pm by Barry Barnett
Areas include these: telecommunications (some of which the Federal Communications Commission oversees), banking (the Federal Reserve); public trading of securities (the Securities and Exchange Commission); air transportation (Federal Aviation Administration); pharmaceuticals and medical devices (Food and Drug Administration); workplace safety (Occupational Safety and Health Administration); and healthcare (Department of Health and Human… [read post]
15 May 2022, 9:11 pm by The Regulatory Review Staff
November 2, 2021 | A Fili-Busted Balance of Power | The filibuster has caused Congress to give up its constitutional power to oversee the administrative state June 9, 2021 | Making Drugs Safe to Kill? [read post]