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26 Mar 2012, 8:07 am
Food and Drug Administration for more safety information about certain hip implant devices that they created. [read post]
24 Mar 2012, 3:09 pm
The Food and Drug Administration’s letter notified DePuy in 2009 that it was turning down the company’s application to sell the device in the United States. [read post]
24 Mar 2012, 7:41 am
In July 2011, the Food and Drug Administration (FDA) issued an update related to what it called 'serious complications' related to the use of vaginal mesh for treatment of pelvic organ prolapse (POP) and stress urinary incontinence (SUI). [read post]
24 Mar 2012, 6:16 am
We are offering free case evaluations to the general public across the United States and Canada. [read post]
24 Mar 2012, 6:14 am
We are offering free case evaluations to the general public across the United States and Canada. [read post]
23 Mar 2012, 3:16 pm
Drugs Let's start with some basic definitions: The Federal Food, Drug, and Cosmetic Act (FD&C Act) and the federal Food and Drug Administration (FDA) define products by their intended use. [read post]
23 Mar 2012, 9:14 am
The appellant, who wishes to be tried in this country, stated first that she admits she would plead guilty to a charge of attempting to import cocaine into the United Kingdom if charged in this jurisdiction. [read post]
23 Mar 2012, 2:59 am
Food and Drug Administration. [read post]
22 Mar 2012, 8:51 am
Food and Drug Administration (FDA), but if approved, thousands of children could suffer Qnexa birth defects. [read post]
22 Mar 2012, 7:43 am
In March 2011, the Food and Drug Administration (FDA) cited safety risks when the organization refused to approve Medtronic's application for a higher dose product similar to Infuse called Amplify. [read post]
22 Mar 2012, 2:59 am
Food and Drug Administration (FDA) first cited concern about cantaloupe safely in 2004. [read post]
21 Mar 2012, 8:09 am
Under the 1984 Hatch-Waxman Act, generic drugmakers were not required to undergo the Food and Drug Administration's (FDA) lengthy approval process if they could prove the generic drug was equivalent to the brand-name medicine. [read post]
21 Mar 2012, 3:00 am
This so-called “death spiral,” in turn, would almost certainly lead to exit of most or all insurers from the relevant market, and there would then be no guarantee of payment for the health-care expenses of those who would have been insured.And, not surprisingly, that has been the experience in those states that attempted such reforms without a minimum coverage provision: guaranteed-issue and community-rating provisions enacted in isolation created a spiral of higher costs and… [read post]
20 Mar 2012, 3:29 pm
” Furthermore, in contrast to the United States, the EU follows a different course: EU Commission officials told us the responsible EU food agency must preapprove the type of food claims that FDA calls structure/function claims before they can be used. [read post]
19 Mar 2012, 3:14 pm
Each year, hundreds of foods and nutritional supplements are recalled in the United States. [read post]
19 Mar 2012, 3:07 pm
Food and Drug Admin., Case No. 11-1482 (D.D.C.) [read post]
19 Mar 2012, 12:41 pm
Food & Drug Administrationet al. [read post]
19 Mar 2012, 12:41 pm
Food & Drug Administrationet al. [read post]
18 Mar 2012, 11:39 am
Food and Drug Administration (FDA) inspected your dietary supplement firm located at 35133 Ravencrest Ct., Yucaipa, CA. [read post]
16 Mar 2012, 12:05 pm
Food and Drug Administration (FDA) has received 1,038 reports of Diabetes Mellitus in Risperdal users. [read post]
