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4 Mar 2011, 1:59 am
Food and Drug Administration. [read post]
1 Jun 2014, 8:12 am
The United States Centers for Disease Control and Prevention (CDC) and Food and Drug Administration (FDA) are also investigating similar cases of Salmonella, and have recalled three sprouted chia seed powder products linked to their investigation after 12 cases were sickened in seven states: Arizona (1), California (2), Connecticut (1), Massachusetts (1), New York (4), Utah (1), and Wisconsin (2). [read post]
FDA Approves First State Drug Importation Program Under 20-Year-Old Statute, But High Hurdles Remain
9 Jan 2024, 7:03 pm
However, before the state can start importing drugs, it must first submit for FDA approval a pre-import request for each eligible prescription drug it plans to import into the United States. [read post]
30 Aug 2010, 2:59 am
Food and Drug Administration recently announced that the agency will hold two public meetings on AquAdvantage Salmon, a genetically modified (GM) Atlantic salmon intended to be used for food, on September 19-21, 2010. [read post]
27 May 2024, 9:05 pm
Although there are on average 2.7 patents per drug, a 2018 study found that each of the 12 top-selling drugs in the United States had on average 71 patents. [read post]
10 Apr 2016, 12:03 pm
Food and Drug Administration for approving the first ever genetically engineered animal for human consumption, a salmon engineered to grow quickly. [read post]
23 Sep 2010, 2:15 pm
The Food and Drug Administration’s decision shows that the Obama administration is taking a harder line on drug safety issues even in the face of scientific uncertainty. [read post]
27 Nov 2009, 4:00 am
In fact, based on a study by the Institute of Medicine in 2007, approximately 1.5 million preventable “adverse drug events” take place in the United States every year. [read post]
4 Nov 2010, 9:00 am
The Food and Drug Administration (FDA) and more than 3,000 state, local, territorial, and tribal agencies work cooperatively to help keep retail food safe throughout the United States. [read post]
11 Jul 2024, 6:43 pm
Laguarta: The United States Food and Drug Administration (FDA) inspected your ready-to-eat (RTE) food manufacturing facility located at 1703 East Voorhees Street, Danville, IL 61834 from December 19, 2023, through February 2, 2024. [read post]
30 May 2024, 9:07 pm
That crisis saw the recall of much of the infant formula in the United States. [read post]
18 Nov 2009, 7:27 am
Louis defective drug attorney, I was disturbed to read about a new Food and Drug Administration warning of potential irreversible cartilage damage from certain anesthetics and medical devices. [read post]
26 Dec 2018, 7:21 pm
The Romaine Lettuce Recall The United States Food & Drug Administration oversees the safety of the nation’s food supply. [read post]
7 Sep 2021, 9:03 pm
Food and Drug Administration, Frank Yiannas, took part in the National Environmental Health Association’s (NEHA) 24-hour live event that was co-hosted with Environmental Health Australia (EHA). [read post]
18 Mar 2011, 2:59 am
Food and Drug Administration said Thursday there is no current need to take potassium iodide pills because of the recent leak of nuclear material in Japan. [read post]
24 May 2015, 10:03 pm
As with previous agendas for the Food and Drug Administration, finalizing the major rules of the Food Safety Modernization Act (FSMA) are a priority. [read post]
7 Feb 2023, 5:48 pm
Food and Drug Administration (FDA) and the Kentucky Cabinet for Health and Family Services Food Safety Branch (CHFS-FSB) jointly inspected your manufacturing facility located at 767 Winchester Road, Lexington, KY 40505-3728 from May 19, 2022, through June 9, 2022. [read post]
14 May 2019, 10:00 pm
Food and Drug Administration’s (FDA) authority to regulate products containing cannabis or cannabis-derived compounds under the Federal Food Drug and Cosmetic Act (FDCA). [read post]
23 Apr 2015, 3:41 pm
On April 21, 2015, the Food and Drug Administration (FDA) issued a notice announcing the availability of a draft guidance document clarifying the Agency’s acceptance of medical device clinical data from studies conducted outside of the United States (“OUS”). [read post]
23 Apr 2015, 3:41 pm
On April 21, 2015, the Food and Drug Administration (FDA) issued a notice announcing the availability of a draft guidance document clarifying the Agency’s acceptance of medical device clinical data from studies conducted outside of the United States (“OUS”). [read post]
