Posts tagged with: "fda" Results 801 - 820 of 40,587
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30 May 2024, 10:02 pm by Bill Marler
The FDA, and likely other states and the CDC are continuing to investigate both a Listeria outbreak that has sickened 2 and a Salmonella Africana outbreak that has now sickened 141. [read post]
30 Sep 2011, 1:33 pm by Brenda Fulmer
  Consumers can also request email updates and an RSS feed from the FDA. [read post]
30 Sep 2011, 1:33 pm by Brenda Fulmer
  Consumers can also request email updates and an RSS feed from the FDA. [read post]
13 Feb 2012, 5:45 am by Morse, Barnes-Brown Pendleton
By: David Fazzolare The long-awaited guidance on biosimilar product development has finally been released by FDA. [read post]
17 Aug 2023, 4:05 am by Howard Friedman
This was the case as to the 2016 action because the FDA did not consider the cumulative effect of the changes it was proposing. [read post]
21 Jan 2015, 11:20 am
Any additional guidance from the FDA is a welcomed development, to the extent that it in any way clarifies the FDA's thinking on regulatory evolving health care delivery technologies. [read post]
15 May 2024, 7:54 am by Bill Marler
Additional Information Post-market Determinations that the Use of a Substance is Not GRAS FDA Update on Post-market Assessment of Certain Food Ingredients Understanding How the FDA Regulates Food Additives and GRAS Ingredients [read post]
6 May 2009, 2:56 am
[December 16, 2008; UPDATED May 05, 2009 - Drug Information Page - FDA] [January 31, 2008 - Healthcare Professional Information Sheet - FDA]"   [read post]
22 May 2015, 10:04 am by Rebecca Tushnet
  IHS alleged that defendants lacked FDA clearance for the “knockoff,” but used the §501(K) number assigned to P-STIM and misrepresented that their device was FDA-approved. [read post]
31 Oct 2023, 11:13 am by Carabin Shaw
Major Brand Product Recalls for Over-the-Counter Eye Drops Issued by FDA The FDA has issued another major product recall after discovering unsanitary practices at major eye drop manufacturing plants. [read post]
1 Mar 2020, 9:00 am by Staff
The post Why the FDA Won’t Approve Your Regenerative Medicine Practice appeared first on Cohen Healthcare Law Group | Healthcare Lawyers | FDA & FTC Law. [read post]
10 Nov 2010, 9:39 pm by Patent Docs
At the center of the issue are the standards that the FDA will require for clinical testing of biosimilars. [read post]
3 Jun 2024, 10:18 am by FRANK VINLUAN - MEDCITY NEWS
Moderna’s mResvia is now the third FDA-approved RSV vaccine and the first one based on mRNA technology. [read post]
15 Dec 2020, 8:45 pm by Staff
The post FDA Approves Authorized Use of a COVID-19 Test Product appeared first on Cohen Healthcare Law Group | Healthcare Lawyers | FDA & FTC Law. [read post]
1 Nov 2020, 9:00 am by Staff
The post Why Medical Device Companies Need to Fear FDA Warning Letters appeared first on Cohen Healthcare Law Group | Healthcare Lawyers | FDA & FTC Law. [read post]