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On March 24, 2016, the US Food and Drug Administration (FDA) published draft guidance to assist applicants who intend to file abbreviated new drug applications (ANDAs) for approval of generic versions of opioid drug products with abuse-deterrent properties. [read post]
16 Aug 2019, 6:49 am by lbergeson@lawbc.com
Department of Health and Human Services (HHS)’s Food and Drug Administration (FDA) announced via the Federal Register the rates for biosimilar user fees for FY 2020. [read post]
6 Aug 2017, 9:00 pm by News Desk
A California bakery and a New York seafood importer are both on notice from the Food and Drug Administration for violations of the federal Food, Drug & Cosmetic Act. [read post]
10 Mar 2022, 7:48 pm by Josh Fensterbush
Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for a ready-to-eat (RTE) chicken salad product containing a Food and Drug Administration (FDA) regulated salad dressing that has been recalled by the producer due to concerns that the salad dressing may contain hard plastic. [read post]
8 Apr 2015, 10:02 pm by News Desk
Food and Drug Administration (FDA) has issued a proposed rule to amend and improve its regulations on food facility registration. [read post]
19 Jul 2024, 8:05 pm by Bill Marler
Food and Drug Administration (FDA) investigated a multistate outbreak of Listeria monocytogenes infections. [read post]
25 Jan 2022, 3:47 am
To effectively tackle the problem of cadmium, arsenic, lead, and mercury in baby food, Congress, the Food and Drug Administration, scientists, the food industry, and medical experts should unite, as the issue concerns our most vulnerable population. [read post]
14 May 2008, 8:32 am
Lawsuit limits have been included in 51 rules proposed or adopted since 2005 by agency bureaucrats governing just about everything Americans use: drugs, cars, railroads, medical devices and food. [read post]
2 Jan 2008, 11:17 am
The Food and Drug Administration has issued a warning about fentanyl pain patches. [read post]
23 Jul 2019, 9:06 pm by Dan Flynn
Food and Drug Administration Tuesday announced it suspended Topway’s food facility registration. [read post]
4 Jan 2017, 10:00 pm by News Desk
Known in the animal pharmaceutical industry as GFI #213, the Food and Drug Administration began the process of implementing the guidance in 2013. [read post]
19 Aug 2011, 8:19 am by info@thomasjhenrylaw.com
Nearly 50%  Food and Drug Administration (FDA) reports of deaths from adverse drug reactions and 61% of hospitalizations from adverse drug reactions were in people younger than 60. [read post]
8 Aug 2021, 9:01 pm by News Desk
As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. [read post]
8 Apr 2011, 10:35 am by rreeves
  The Food and Drug Administration unveiled its new website, which boasts of an easy-to-search-for tabular format for consumers to search for food recalls. [read post]
5 Oct 2014, 10:03 pm by News Desk
Food and Drug Administration (FDA) officials recently sent warning letters to owners of a pizza dough and cheese grating/repackaging facility in NY, a fortune cookie manufacturing plant in GA, a rice storage/milling facility in FL, two dairies in NY and one in OH. [read post]
20 Nov 2022, 9:01 pm by News Desk
As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. [read post]
20 Mar 2012, 1:54 pm by Olivia
In November, TeenJury reported on a temporary halt to the Food and Drug Administration’s plan to require that cigarette manufacturers place graphic warning labels on their packaging. [read post]
1 Sep 2011, 11:15 am
Food and Drug Administration (FDA) report concluded that implanted transvaginal mesh failed to result in better outcomes than non-mesh surgeries. [read post]
6 May 2011, 1:17 pm
Food and Drug Administration's continued approval of this 50-year-old defective product. [read post]
31 Oct 2010, 11:29 am by Larry Jones
The federal Food & Drug Administration has announced a nationwide recall of seven lots of Heparin injaction products at the healthcare provider level due to the presence of of oversulfated chondroitin sulfate contaminate. [read post]