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29 Jan 2016, 12:32 am
Food and Drug Administration (FDA), and the Public Health Agency of Canada to investigate a multistate outbreak of Listeria monocytogenes infections (listeriosis). [read post]
28 Jan 2016, 10:00 pm
Food and Drug Administration does not require labeling food processed with genetic engineering because the agency says no food safety issue is involved. [read post]
28 Jan 2016, 2:49 pm
“Voluntary recall is a specific term used by the Food and Drug Administration. [read post]
28 Jan 2016, 2:24 pm
Food and Drug Administration (FDA), and the Public Health Agency of Canada to investigate a multistate outbreak of Listeria monocytogenes infections (listeriosis). [read post]
28 Jan 2016, 11:40 am
In the United States, at least 2 million antibiotic-resistant illnesses and 23 000 deaths occur each year, at a cost to the U.S. economy of at least $30 billion (2). [read post]
28 Jan 2016, 6:18 am
As noted in the article, the United States Food and Drug Administration (FDA) is on the verge of approving a reversal agent (antidote) for Xarelto that was manufactured by the makers of Pradaxa. [read post]
27 Jan 2016, 11:54 pm
The Public Health Agency of Canada is collaborating with federal and provincial public health partners, the United States Centers for Disease Control and Prevention (CDC), and the United States Food and Drug Administration (FDA) to investigate an outbreak of Listeria monocytogenes infections linked to Dole packaged salad products produced from a US processing facility in Springfield, Ohio. [read post]
27 Jan 2016, 10:03 pm
Food and Drug Administration (FDA) charged the company with partially distributing the shipment into U.S. commerce “for consumption without an FDA release. [read post]
26 Jan 2016, 10:02 pm
This is the same outbreak where the Food and Drug Administration (FDA) traceback investigation ended up at the Rancho Don Juanito de R.L. de C.V. located in Baja, Mexico as the source of the contaminated cucumbers that were then shipped into the United States via a San Diego produce distributor. [read post]
25 Jan 2016, 2:53 am
Food and Drug Administration (FDA) to investigate a multistate outbreak of Listeria monocytogenes infections (listeriosis). [read post]
22 Jan 2016, 7:43 pm
All states have regulations requiring health care providers to report cases of listeriosis and public health officials try to interview all persons with listeriosis promptly using a standard questionnaire about high-risk foods. [read post]
21 Jan 2016, 9:45 pm
Food and Drug Administration (FDA) published draft guidance that provides medical device companies with recommendations to prevent security breaches when medical devices are in use, and encourages those companies to develop methods for managing cybersecurity risk. [read post]
20 Jan 2016, 10:04 pm
United States v. 39 Cases, 192 F. [read post]
20 Jan 2016, 2:39 pm
Food and Drug Administration found to be inadequate.... [read post]
19 Jan 2016, 6:41 am
Your lawyer will need an expert witness who is familiar with the requirements of the United States Food and Drug Administration (FDA) that pertain to medical devices, as well as having knowledge of production techniques and medical device marketing regulations. [read post]
17 Jan 2016, 10:02 pm
Three U.S. dairy farms and two food importers were on the receiving end of warning letters recently from the Food and Drug Administration. [read post]
17 Jan 2016, 10:01 pm
And he points to leading-edge technology that is helping raw-milk dairies embrace better food-safety practices — such as a type of rapid-test science approved by the Food and Drug Administration. [read post]
17 Jan 2016, 6:41 am
The United States Food and Drug Administration (FDA) has recently issued a press release dealing with new changes to regulations regarding the use of transvaginal mesh (TVM) implants. [read post]
15 Jan 2016, 7:51 am
We now know that the drug company did not do enough testing to establish and did not disclose what data they had provided to the United States Food and Drug Administration (FDA). [read post]
14 Jan 2016, 10:05 pm
Food and Drug Administration (FDA) issued a notice that it will be holding a public workshop to receive comments from the healthcare industry and the public about genetic testing, including when it should be used and the appropriate method for providing results to patients. [read post]
