Search for: "UNITED STATES FOOD & DRUG ADMINISTRATION " Results 3981 - 4000 of 6,135
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2 Aug 2012, 2:31 am by tekEditor
There are many stereotypes in Germany about life in the United States. [read post]
31 Jul 2012, 4:00 am by ipelton
Patent and Trademark Office, and Small Business Administration (SBA), along with other agencies, address this issue. [read post]
30 Jul 2012, 12:49 pm by Cal Warriner
So when Smith & Nephew applied to have its Birmingham Hip Resurfacing System (BHR), metal-on-metal (MoM) hip implant approved by the Food and Drug Administration, Wright tried to block the approval. [read post]
30 Jul 2012, 12:16 pm by bradhendrickslawfirm
In 2008, the United States Food and Drug Administration (“FDA”) issued a Public Health Notification (“PHN”) to warn patients about adverse effects related to urogynecologic use of surgical mesh. [read post]
30 Jul 2012, 12:16 pm by bradhendrickslawfirm
In 2008, the United States Food and Drug Administration (“FDA”) issued a Public Health Notification (“PHN”) to warn patients about adverse effects related to urogynecologic use of surgical mesh. [read post]
30 Jul 2012, 12:16 pm by bradhendrickslawfirm
In 2008, the United States Food and Drug Administration (“FDA”) issued a Public Health Notification (“PHN”) to warn patients about adverse effects related to urogynecologic use of surgical mesh. [read post]
30 Jul 2012, 2:59 am
   However, the United States Food and Drug Administration warns against drinking raw milk, saying that it can contain harmful, or even potentially deadly bacteria, such as E. coli O157:H7, Salmonella and Campylobacter. [read post]
29 Jul 2012, 8:33 am by FDABlog HPM
Customs and Border Protection, FBI, Food and Drug Administration’s Office of Criminal Investigations, and “countless state and local law enforcement members in more than 109 cities. [read post]
27 Jul 2012, 5:50 pm
Although Merck reportedly informed the nation's Food and Drug Administration (FDA) that some men experienced sexual side effects during clinical trials, the FDA's website reports those side effects went away after patients stopped using the drug. [read post]
27 Jul 2012, 12:40 pm by Meyer Glitzenstein & Crystal
  In this round, the companies argued that the district court’s findings and remedies in connection with their 50-years of fraud should be set aside in light of the 2009 legislation which gave the Food and Drug Administration authority to regulate cigarettes. [read post]
27 Jul 2012, 9:30 am
The plaintiffs argued that the generic drug manufacturers should be liable because the manufacturers 1) failed to warn about the risks associated with long-term use of the drug; 2) failed to request a labeling change revision with the United States Food and Drug Administration (FDA) as provided under the FDCA's "Changes Being Effected" provisions; and 3) failed to report safety information to the medical community. [read post]
27 Jul 2012, 1:21 am by FDABlog HPM
” Cytori claims that FDA’s refusal to clear the devices for distribution in the United States is thus arbitrary and capricious. [read post]
26 Jul 2012, 2:40 pm by Charles Johnson
The drug had been shipped from China. 2008: First seizure of MDPV in the United States. 2009: MDPV made illegal in Denmark. 2010: MDPV made a controlled drug in the UK, Sweden, Germany, Australia and Finland. [read post]
26 Jul 2012, 1:37 pm by admin
FDA Adverse Effects Reports The Food and Drug Administration  has received more than 3,800 reports of significant complications associated with transvaginal mesh patches. [read post]
26 Jul 2012, 7:02 am
A United States attorney called the settlement "unprecedented in both size and scope. [read post]
25 Jul 2012, 8:19 pm by FDABlog HPM
  On Monday, the United State District Court for the District of Columbia ruled in favor of FDA and granted its motion for summary judgment and issued a permanent injunction against the use of the Regenexx Procedure. [read post]
25 Jul 2012, 5:56 pm
Food and Drug Administration report in August 2011 found vaginal-mesh products should be classified as high risk to patients based on a review of side-effect reports from January 2008 to December 2010. [read post]
25 Jul 2012, 5:56 pm
Food and Drug Administration report in August 2011 found vaginal-mesh products should be classified as high risk to patients based on a review of side-effect reports from January 2008 to December 2010. [read post]
24 Jul 2012, 2:59 am
Food and Drug Administration (FDA)," Antolinez said. [read post]
23 Jul 2012, 12:00 pm by Lucas A. Ferrara, Esq.
The pills were ultimately sold to wholesale prescription drug distribution companies ("corrupt distribution companies"), which then sold them to pharmacies and to other wholesale prescription distribution drug companies across the United States. [read post]