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22 May 2023, 9:05 pm by Dan Flynn
Eleven organizations that work closely with the Food and Drug Administration are asking bipartisan congressional leaders to work with them on “several pressing food safety issues this year. [read post]
9 Jun 2022, 4:45 pm by Lawrence Solum
  Here is the abstract: This Article argues that the Food and Drug Administration (“FDA”) should regulate drug manufacturer speech about off-label uses based on the evidentiary support for the relevant use. [read post]
3 Jun 2024, 9:09 am by News Desk
According to details published online by the Food and Drug Administration (FDA), the recall was initiated May 17, 2024, and is ongoing. [read post]
– Opinion – In recent days, the Food and Drug Administration released the 2020 Summary Report on Antimicrobials Sold or Distributed for Use in Food-Producing Animals, which showed sales levels close to those from recent years. [read post]
31 Mar 2007, 10:36 am
Here's an excerpt:The Food and Drug Administration said yesterday that it had not found rat poison in pet food that has... [read post]
6 Feb 2008, 9:54 am
Federal Oversight of Food Safety: FDA's Food Protection Plan Proposes Positive First Steps, but Capacity to Carry Them Out Is Critical Summary (from GAO) The Food and Drug Administration (FDA) is responsible for ensuring the safety of roughly 80 percent... [read post]
12 Feb 2008, 6:44 am
From a CFSAN Constituent Update: The Food and Drug Administration (FDA) today [Feb. 7, 2008] issued draft compliance policy guidance on Listeria monocytogenes (L. monocytogenes) in ready-to-eat (RTE) foods, and draft guidance for the industry on controlling the food-borne pathogen... [read post]
16 Feb 2016, 7:22 am by Robert Kraft
The Washington Post reports in “Wonkblog” that two new studies raise concerns about the 21st Century Cures Act’s reforms to speed up the Food and Drug Administration’s drug approval process. [read post]
5 Oct 2007, 10:29 am
The US Food and Drug Administration (FDA) today announced a new program aimed at speeding up the approval process for generic drugs. [read post]
11 May 2007, 8:15 am
The Food and Drug Administration ordered drug makers yesterday to add warnings to antidepressant medications, saying the drugs increase the risk of suicidal thinking or behavior in some young adults. [read post]
5 Oct 2011, 5:52 pm
Food and Drug Administration seeking mandatory labeling for foods made from genetically engineered crops, a move long opposed by biotech companies.Andrew Kimbrell, executive director of the Center for Food Safety (CFS), stated that, "they should label the foods and let consumers know. [read post]
25 Mar 2009, 9:15 pm
A former deputy commissioner for policy at the Food and Drug Administration (FDA) is among those who support the idea of stripping food safety responsibility from the agency and creating a new Food Safety Administration within the Department of Health and Human Services. [read post]
8 Jul 2010, 2:59 am
Food and Drug Administration (FDA) food safety reform since early 2009, when his Administration launched the Food Safety Working Group.In the statement President Obama noted the Food Safety Working Group, chaired by Health and Human Services Secretary Kathleen Sebelius and Secretary of Agriculture Tom Vilsack, has issued recommendations on how to upgrade the food safety system and he outlined a few of the actions the… [read post]
30 Jul 2013, 1:34 pm by Ronald V. Miller, Jr.
In addition to the European agency, the Food and Drug Administration has been reviewing the safety of a big class of drugs that includes Januvia by Merck and the drugs Byetta, Bydureon and Onglyza, which are sold by Bristol-Myers Squibb and AstraZeneca. [read post]
30 Jul 2013, 1:34 pm by Ronald V. Miller, Jr.
In addition to the European agency, the Food and Drug Administration has been reviewing the safety of a big class of drugs that includes Januvia by Merck and the drugs Byetta, Bydureon and Onglyza, which are sold by Bristol-Myers Squibb and AstraZeneca. [read post]
30 Jul 2013, 1:34 pm by Ronald V. Miller, Jr.
In addition to the European agency, the Food and Drug Administration has been reviewing the safety of a big class of drugs that includes Januvia by Merck and the drugs Byetta, Bydureon and Onglyza, which are sold by Bristol-Myers Squibb and AstraZeneca. [read post]
30 Jul 2013, 1:34 pm by Ronald V. Miller, Jr.
In addition to the European agency, the Food and Drug Administration has been reviewing the safety of a big class of drugs that includes Januvia by Merck and the drugs Byetta, Bydureon and Onglyza, which are sold by Bristol-Myers Squibb and AstraZeneca. [read post]
22 Apr 2010, 5:02 am by Mark Zamora
The United States Food and Drug Administration (FDA) has added a Boxed Warning to the label for propylthiouracil, a drug used to treat hyperthyroidism (overactive thyroid), to include information about reports of severe liver injury and acute liver failure, some of which have been fatal, in adult and pediatric patients using this medication.The new warning also states that for patients being started on treatment for hyperthyroidism it may be appropriate to reserve… [read post]
30 Jan 2010, 3:55 am by Dan Frith
My bet is that you do know someone like this...maybe several someones.The Wall Street Journal, quoting Food and Drug Administration (FDA) data, recently reported that medication errors cause at least one death every day and injure approximately 1.3 million people annually in the United States. [read post]
7 Sep 2011, 7:17 am by Breakstone, White & Gluck
A Food and Drug Administration (FDA) panel will begin discussing the safety and effectiveness of urogynecologic mesh products Wednesday. [read post]