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FDA

we are not treating our disease, but merely building health

From: Karl
Sent: Wednesday, March 10, 2010 2:46 PM
To: Lloyd
Subject: fda taking time and energy to police..... YOU?!

With big tobacco, Chinese toxic products and other blatant public safety crisis  flooding the marketplace, it is disgusting that the FDA is finding the resources to micro-manage your website semantics. They really are screaming to the world that they are working for big pharma and not consumers. I am disappointed Obama has not taken steps to correct some of the most egregious fascist policy. I am disappointed that our present Canadian government is following America blindly. For many years we had an independent Canadian government.

FDA Requires Updated Labeling for Interferon Alpha Products Due to Identified Safety Issues:

Each approved alpha interferon product will now include statements regarding possible risk of

FDA Issues Dietary Supplements Final Rule (2007)

FDA NEWS RELEASE

FOR IMMEDIATE RELEASE
June 22, 2007

Media Inquiries:
Michael Herndon and Kimberly Rawlings, 301-827-6242
Consumer Inquiries:
888-INFO-FDA

What will we do if they are successful…?

Ltr to Lloyd jan – feb2010

Dear Lloyd,

Sorry not to have replied sooner, but I have been swamped with things on several fronts, and am still trying to catch up with my course work and everything else I put on hold since I got my diagnosis in December...!  It's like trying to crawl out of a big abyss !! :-o

Senator McCain Files New Bill That Attacks Your Access to Supplements and Repeals Key Sections of the Dietary Supplement Health

This is a Full Court Press From Those Who Want to Implement CODEX.
It MUST BE FOUGHT NOW!  Click Here and Get on Board

Track This Bill HERE

McCain’s bill is called The Dietary Supplement Safety Act (DSSA). It would repeal key sections of the Dietary Supplement Health and Education Act (DSHEA). DSHEA protects supplements if 1) they are food products that have been in the food supply and not chemically altered or 2) if they were sold as supplements prior to 1994, the year that DSHEA was passed. If a supplement fits one of these two descriptions, the Food and Drug Administration (FDA) cannot arbitrarily ban it or reclassify it as a drug.

These protections are far from perfect. They discourage companies from developing new forms of supplements. New supplements may be arbitrarily banned by the FDA or adopted by drug companies in a way that precludes their further sale as supplements.

McCain’s bill would wipe out even the minimal protections contained in DSHEA. It would give the FDA full discretion and power to compile a discreet list of supplements allowed to remain on the market while banning all others.  
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