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16 Mar 2012, 11:00 am
In August, 2011 Del Monte sued the Food and Drug Administration (FDA) to seek an injunction that would lift an FDA ban restricting the importation of whole, fresh cantaloupes into the United States. [read post]
16 Mar 2012, 11:00 am
In August, 2011 Del Monte sued the Food and Drug Administration (FDA) to seek an injunction that would lift an FDA ban restricting the importation of whole, fresh cantaloupes into the United States. [read post]
15 Mar 2012, 2:21 pm
Food and Drug Administration (FDA) through its 510(k) process, a fast track to market process. [read post]
14 Mar 2012, 2:03 pm
Food and Drug Administration who now consults for the food industry, said the results of CDC's review were not all that surprising considering the United States is not only importing more food, but more high risk items like seafood, spices and produce.According to the U.S. [read post]
13 Mar 2012, 7:14 pm
These violations cause your drug products to be adulterated within the meaning of section 501(a)(2)(B) of the Federal Food, Drug, and Cosmetic Act (the Act) [21 U.S.C. [read post]
13 Mar 2012, 10:06 am
If a product is labeled, promoted or used in a manner that meets the following definition in section 201(h) of the Federal Food Drug & Cosmetic (FD&C) Act it will be regulated by the Food and Drug Administration (FDA) as a medical device and is subject to premarketing and postmarketing regulatory controls. [read post]
13 Mar 2012, 2:59 am
Food and Drug Administration to take greater leadership on the issue. [read post]
12 Mar 2012, 8:41 am
Food and Drug Administration. [read post]
12 Mar 2012, 8:38 am
In January of 2012, the Food and Drug Administration stated that the labels on Yasmin and Yaz needed to be stronger and that more information needed to be given about the medication possibly causing blood clots for women. [read post]
12 Mar 2012, 8:37 am
In 2003, the Food and Drug Administration began stating their concerns over the rate of blood clots developing in women who took Yaz. [read post]
12 Mar 2012, 4:17 am
Food and Drug Administration, European Food Safety Authority and Health Canada, consider caramel coloring safe for use in foods and beverages. [read post]
10 Mar 2012, 11:35 am
The drug was approved for use in the United States in October 2010, and it has a high number of adverse-event reports. [read post]
9 Mar 2012, 9:38 pm
And the federal Food and Drug Administration (FDA) did just that, recently requiring that all cigarette advertising carry graphic warnings on their packaging, similar to that required in Europe. [read post]
9 Mar 2012, 12:17 pm
Patients suffering from atrial fibrillation normally require a blood-thinning agent such as warfarin, which for over 60 years was the only Food and Drug Administration (FDA) approved medicine until Pradaxa entered the market. [read post]
8 Mar 2012, 5:39 pm
Food and Drug Administration warn consumers some illegal skin cream, beauty and antiseptic soaps from abroad may contain mercury.Gary Coody, national health fraud coordinator at the FDA's Office of Regulatory Affairs said the products, marketed as skin lighteners and anti-aging treatments that remove age spots, freckles, blemishes and wrinkles, were manufactured abroad and sold illegally in the United States. [read post]
8 Mar 2012, 7:25 am
In the United States, an estimated 120 deaths have been blamed on Pradaxa serious bleeding events. [read post]
6 Mar 2012, 9:30 am
Food and Drug Administration. [read post]
They need to hear our stories - A Broken System - Shock and Anger - Disheartened - Left to Speculate
5 Mar 2012, 4:08 pm
” The report also made it clear that the public was not welcome: The meetings are open to growers, buyers, auditors, academic experts, as well as regulators from state agencies, the Food & Drug Administration and the U.S. [read post]
5 Mar 2012, 12:49 pm
Food and Drug Administration (FDA) to reject Johnson & Johnson’s sale of an artificial hip in the U.S., but it didn’t stop the company from marketing it in Europe, according to a recent article by the New York Times. [read post]
4 Mar 2012, 10:55 pm
Food and Drug Administration (FDA) has found that these surgical meshes can harm patients and put them at risk for serious side effects including: Severe pain Mesh erosion Additional surgeries Infection Bleeding Organ perforation Neuro-muscular problems Vaginal scarring Mesh contraction Vaginal shortening/shrinking According to FDA reports, in 2010, approximately 300,000 women underwent surgical procedures in the… [read post]
