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15 Nov 2020, 7:17 am
The Food and Drug Administration (FDA) recently gave approval to the first new mesothelioma drug treatment combination for patients in the last 16 years. [read post]
31 Jan 2013, 9:00 am
., Board Certified by The Florida Bar in Health Law A Food and Drug Administration (FDA) advisory committee voted 19 to 10 in favor of moving hydrocodone combination drugs from schedule III into the more restrictive schedule II category of controlled substances. [read post]
31 Jan 2013, 9:00 am
., Board Certified by The Florida Bar in Health Law A Food and Drug Administration (FDA) advisory committee voted 19 to 10 in favor of moving hydrocodone combination drugs from schedule III into the more restrictive schedule II category of controlled substances. [read post]
31 Jan 2013, 9:00 am
., Board Certified by The Florida Bar in Health Law A Food and Drug Administration (FDA) advisory committee voted 19 to 10 in favor of moving hydrocodone combination drugs from schedule III into the more restrictive schedule II category of controlled substances. [read post]
6 Apr 2020, 3:36 pm
Food and Drug Administration issued a news release requesting manufacturers to withdraw all products containing the popular heartburn drug, ranitidine, the active ingredient in the medication, Zantac. [read post]
4 Aug 2016, 7:35 pm
., Commissioner of Food and Drugs, Food and Drug Administration, FDA, that, as a result of an ongoing audit his office was conducting, it was found that the method that the FDA used to initiate a food recall was inefficient and ineffective.The post FDA Food Recall System is Broken appeared first on Legal Reader. [read post]
28 Sep 2018, 2:47 am
The Food and Drug Administration does not regulate labeling for wine containing over 7% of alcohol. [read post]
8 Jul 2022, 5:05 am
The post The Food & Drug Administration Has a Vaping Problem appeared first on Reason.com. [read post]
12 Oct 2010, 1:19 pm
Like it or not, the Food & Drug Administration is in a constant conflict of interest. [read post]
14 May 2013, 10:00 am
On May 8, 2013, the US Food and Drug Administration (FDA) sent a warning to doctors and pharmacists to avoid drugs made by The Compounding Shop, based in St. [read post]
14 May 2013, 10:00 am
On May 8, 2013, the US Food and Drug Administration (FDA) sent a warning to doctors and pharmacists to avoid drugs made by The Compounding Shop, based in St. [read post]
14 May 2013, 10:00 am
On May 8, 2013, the US Food and Drug Administration (FDA) sent a warning to doctors and pharmacists to avoid drugs made by The Compounding Shop, based in St. [read post]
5 Apr 2009, 10:09 pm
National Library of Medicine of the National Institutes of Health has digitized the Food and Drug Administration's Notices of Judgment Collection, 1906-1963. [read post]
2 Mar 2022, 9:02 pm
The food and Drug Administration is investigating four ongoing foodborne illness outbreaks. [read post]
15 Aug 2016, 7:17 am
FDA issued a draft revised guidance for industry, “General Principles for Evaluating the Human Food Safety of New Animal Drugs Used In Food-Producing Animals” in July 2016 that “described the type of information that the Food and Drug Administration’s (FDA’s) Center for Veterinary Medicine (CVM) recommends sponsors provide [the agency] to address the human food safety of new animal drugs used in… [read post]
17 Jul 2015, 12:43 pm
The final rule implements provisions of the Food and Drug Administration Safety and Innovation Action of 2012 (FDASIA) (Pub. [read post]
15 Jul 2007, 7:02 am
Food and Drug Administration (FDA). [read post]
17 Feb 2009, 4:03 am
Titled "Opportunities and Challenges Facing FDA & the New Administration," the Food & Drug Law Institutes's Annual Conference will focus on changes under President Obama's new administration. [read post]
21 Oct 2013, 10:00 am
., Board Certified by The Florida Bar in Health Law On September 20, 2013, the US Food and Drug Administration (FDA) announced that companies will have to include unique device identification (UDI) codes on medical devices. [read post]
21 Oct 2013, 10:00 am
., Board Certified by The Florida Bar in Health Law On September 20, 2013, the US Food and Drug Administration (FDA) announced that companies will have to include unique device identification (UDI) codes on medical devices. [read post]
