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13 Jul 2017, 1:42 pm
A New York-based expert on mitochondrial depletion syndrome gave evidence to the court via video link – telling them that he believes an experimental drug available in the U.S. provided the F.D.A. approves its use – has a 10 percent chance of improving the boy’s health. [read post]
31 Mar 2017, 1:50 pm
The same NYT news story provides some contextual information which seems to help understand that issue: A spokeswoman for the F.D.A., Stephanie Caccomo, said Tuesday’s announcement was made because “in 2016, there were several advances in the description of the disease and treatment recommendations, including recognition of the disease by the World Health Organization and publication of diagnosis and treatment guidelines by the Plastic Surgery Foundation and National… [read post]
14 Mar 2017, 6:01 pm
Neuman last year also penned – “As Cheesemaking Blooms, So Can Listeria” and “Small Cheesemaker Defies F.D.A. [read post]
17 Feb 2017, 7:19 am
’ ‘The bottom line for us is that milk is defined by the F.D.A., and we’re saying to the F.D.A.: Enforce your definition,’ Mr. [read post]
29 Jul 2016, 8:06 am
Neuman also penned – “As Cheesemaking Blooms, So Can Listeria” and “Small Cheesemaker Defies F.D.A. [read post]
25 Jul 2016, 7:01 am
” As an alternative, the industry has proposed a cooperative effort between generic drug makers and brand-name companies “that would make the F.D.A. the final arbiter of label changes. [read post]
20 May 2016, 3:00 am
” According to the report, Pfizer’s announcement means that all F.D.A. [read post]
20 May 2016, 3:00 am
” According to the report, Pfizer’s announcement means that all F.D.A. [read post]
6 Apr 2016, 11:08 am
New York Times (Apr. 2, 2016): Arizona Governor Signs Abortion Bill that Skirts F.D.A. [read post]
10 Mar 2016, 8:56 am
According to a citizens’ petition filed with the F.D.A., an inspector was given records of 16,047 complaints made to the original manufacturer, Conceptus, between 2011 and 2013, when Bayer acquired a majority interest in the company. [read post]
10 Mar 2016, 8:56 am
According to a citizens’ petition filed with the F.D.A., an inspector was given records of 16,047 complaints made to the original manufacturer, Conceptus, between 2011 and 2013, when Bayer acquired a majority interest in the company. [read post]
10 Mar 2016, 8:56 am
According to a citizens’ petition filed with the F.D.A., an inspector was given records of 16,047 complaints made to the original manufacturer, Conceptus, between 2011 and 2013, when Bayer acquired a majority interest in the company. [read post]
10 Mar 2016, 8:56 am
According to a citizens’ petition filed with the F.D.A., an inspector was given records of 16,047 complaints made to the original manufacturer, Conceptus, between 2011 and 2013, when Bayer acquired a majority interest in the company. [read post]
1 Mar 2016, 7:00 am
Additional Resources: F.D.A. [read post]
22 Feb 2016, 5:01 am
Shumlin has placed the blame for that crisis at the feet of the Food and Drug Administration (F.D.A.) and pharmaceutical industry, which together have enabled pain management practices that in 2012 resulted in the issuing of enough opiate prescriptions to give every American their own bottle of pills. [read post]
27 Jan 2016, 7:47 am
The New York Times reports that a Food and Drug Administration report issued to Congress concludes that “patients have been demonstrably harmed or may have been harmed by [laboratory-developed] tests that did not meet F.D.A. requirements. [read post]
27 Oct 2015, 7:06 am
According to the Times, the findings “could bolster support for the F.D.A. [read post]
14 Oct 2015, 10:26 am
“The very high rate of reoperations — 10 times as high with Essure — is likely to add to concerns about the accuracy of the clinical trial data provided to the F.D.A. [read post]
24 Aug 2015, 7:53 am
According to the New York Times, the decision “could inhibit the ability of the F.D.A. to regulate one aspect of pharmaceutical marketing. [read post]
9 Aug 2015, 4:26 am
However, as our Boston Xarelto injury attorneys can explain, there is a new antidote undergoing the F.D.A. approval process; however, it is not yet available to the patients currently taking one of the potentially dangerous new drugs. [read post]
