Fake Medical Product Gets Approval for Testing
Submitted by Jason Ramsey on Fri, 03/27/2009 - 15:28The Government Accountability Office in a sting operation found lax screening by review boards and this would now result in stricter regulations for medical research groups that monitor clinical trials.
Food Safety Systems Need Reform says Report
Submitted by Amit Pathania on Thu, 03/26/2009 - 12:27A new report Keeping America's Food Safe: A Blueprint for Fixing the Food Safety System was released by Trust for America's Health (TFAH) and the Robert Wood Johnson Foundation (RWJF) which said immediate consolidation of food safety leadership within the Food and Drug Administration (FDA) was needed.
Judge orders FDA to allow over-the-counter availability of Plan B to 17-year-olds
Submitted by Jason Ramsey on Tue, 03/24/2009 - 13:40The Food and Drug Administration decision of restricting the over-the-counter availability of the Plan B morning-after pill to the 17-year-olds has been denounced by Eastern District of New York Judge Edward R. Korman.
FDA gives approval to treatment-resistant depression drug Symbyax
Submitted by Jason Ramsey on Mon, 03/23/2009 - 19:54New drug, Symbyax got approval of the Food and Drug Administration as a therapy for treatment-resistant depression.
Drug developer Eli Lilly & Co said that Symbyax is the first drug approved by FDA for the acute treatment of treatment-resistant depression, which involves two failed attempts with other anti-depressants.
Dispute over Solodyn ended by Medicis and Teva
Submitted by Amit Pathania on Thu, 03/19/2009 - 15:37Israel's Teva Pharmaceutical Industries Ltd, which is the world's largest generic drug maker, announced on Wednesday that they have received final approval from the U. S. Food and Drug Administration, FDA for their Abbreviated New Drug Application, or ANDA, to market the generic version of acne drug Solodyn or Minocycline HCl, Extended-Release Tablets, 45 mg, 90 mg and 135 mg.
Modest Risk from Chemicals found in Baby Toiletries
Submitted by Jason Ramsey on Mon, 03/16/2009 - 20:44According to a report called No More Toxic Tub from the Campaign for Safe Cosmetic Use many baby and child-care products contain the chemicals formaldehyde and
1,4-dioxane which carry cancer and skin condition risks and these products aren't listed on the labels.
Obama picks Margaret Hamburg as FDA chief; intends forming a Food Safety Working Group
Submitted by Jason Ramsey on Mon, 03/16/2009 - 01:36According to Associated Press reports, in his weekly radio address Saturday, President Obama put forth his picks for the posts of FDA Commissioner and Deputy Commissioner. As expected, he named Margaret Hamburg – the New York City Health Commissioner - for the top FDA post; and Joshua Sharfstein - Baltimore Health Commissioner - as her principal deputy.
Female Condom FC2 gets FDA’s Nod
Submitted by Jason Ramsey on Fri, 03/13/2009 - 08:58The Food and Drug Administration has approved a lower-cost new version of the female condom, called the FC2 Female Condom for sale in the U.S. after an advisory panel endorsed the product late last year.
Many Baby Products Contain Probable Carcinogens
Submitted by Jason Ramsey on Fri, 03/13/2009 - 06:27A consumer group has said that many baby and child care products contain the chemicals formaldehyde and 1,4-dioxane, both of which have been linked to cancer and various skin conditions but the labels don’t list them.
Obama picks ex-NYC health commissioner Margaret Hamburg to lead FDA
Submitted by Aaron Ross on Thu, 03/12/2009 - 10:53President Barack Obama is likely to hand over that reins of the distraught FDA - Food and Drug Administration - to Margaret A. Hamburg, an ex-Health Commissioner, New York City. Obama's pick for the FDA's Deputy Commissioner is Joshua Sharfstein, the Baltimore Health Commissioner.
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