(NaturalNews) The United States Department of Health and Human Services is reporting that Cesareans are on the rise up 53 percent since 1996. lawmakers began inquiring, the department finally admitted that, yes, orders for billions of rounds indeed have been placed, but only as a means of saving money.
The FDA is run by unelected bureaucrats who answer to no one and write their own "laws, (See attorney Jonathan Emord's book The Rise of Tyranny to learn more.)&bull; The FDA can <a href=temp.rcgov.org/planning/></a> simply choose to DENY all applications and thereby outlaw virtually all nutritional supplements.
Be less critical. The odds against that happening are astronomical.The other option is to just wait for the current U.S. We need a new energy. is considered highly substandard. Roughly 11 percent of patients who received the NicVAX shot quit smoking, but the same amount from the placebo group also quit smoking -- in other words, there was no difference at all in quit rates between the two groups.Upon news of the failed Phase III trial, Nabi's stock price dropped a massive 70 percent, and GSK's dropped about one percent.
A proposal to begin a clinical trial of this adhesive gel on humans was submitted to an FDA-recognized IRB company, and the company approved it! This, despite the fact that the clinical trial called for pouring one liter of this adhesive gel into the stomach of patients.Misleading the misleadersThe IRB that fell for the ruse was Coast IRB, LLC of Colorado Springs, which after being caught, charged that the GAO investigators violated federal law by misrepresenting themselves when they submitted false credentials to the review company.But isn't this exactly what a medical review company is supposed to notice and prevent in the first <a href=www.saysandiego.org/form/>lululemon</a> place? This company seems to think they can trust everything they're told by any person or company applying for review, regardless of whether the medical products in question make any sense at all.Coast IRB is one of 6,300 IRBs (Independent Review Boards) that certify pharmaceutical trials and medical device trials for consideration by the FDA.The next time you considering using an "FDA-approved" medical device or pharmaceutical, remember this simple truth: In America, the Department of Health and Human Services will certify a fictitious review company headed by a dog!If the GAO can pull this off after running the sting on just 3 companies, imagine how many of the 6,300 IRBs are certifying fraudulent, dangerous or outright deadly medical devices and pharmaceuticals right now!What this fiasco really <a href=roxie.com/common/tags/>Cheap Lululemon</a> shows is that the medical device oversight system in America today is a complete joke
In a statement, FDA Commissioner Margaret Hamburg said that Avastin has never been proven to be safe or effective, but also in the same breath noted that doctors can still prescribe the drug if they feel like it,FDA recognizes how hard it is for <a href=www.farmissues.com/photos/index.cfm>Lululemon Headbands</a> patients and their families to cope with metastatic breast cancer and how great a need <a href=www.mbsports.net/dealers/>lululemon Headbands</a> there is for more effective treatments, Hamburg is quoted as saying by The Pittsburgh Tribune-Review.
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