By Alfred Lambremont Webre, JD, MEd
September 30, 2011 is the deadline for public comment on the Food and Drug Administration’s “Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues” that - unless stopped by public pressure and refusal - will go into effect December 31, 2011.
According to several experts, the FDA document, introduced in stealth over the July 4, 2011 weekend, and masked with deceptive language, is the tool for the roll-out of the CODEX ALIMENTARIUS in the U.S., the New World Order plan to weaponize food and support a NWO plan to populate between 1/3-2/3 of the Earth’s population or more by various stealth means, including the weaponization of food.
One expert states, “We have reviewed the very complicated new regulations in detail. In the hands of an agency charged with regulating supplements fairly—one not hostile to supplements the way FDA is—they might be made to work. But in the hands of the FDA, which wants everything, supplements and drugs alike, to go through the vastly expensive new drug approval process, we fear the new rules will be used to forbid the development or sale of any new supplements—where “new” means anything after 1994, when DSHEA was passed.
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September 30, 2011 is the deadline for public comment on the Food and Drug Administration’s “Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues” that - unless stopped by public pressure and refusal - will go into effect December 31, 2011.
According to several experts, the FDA document, introduced in stealth over the July 4, 2011 weekend, and masked with deceptive language, is the tool for the roll-out of the CODEX ALIMENTARIUS in the U.S., the New World Order plan to weaponize food and support a NWO plan to populate between 1/3-2/3 of the Earth’s population or more by various stealth means, including the weaponization of food.
One expert states, “We have reviewed the very complicated new regulations in detail. In the hands of an agency charged with regulating supplements fairly—one not hostile to supplements the way FDA is—they might be made to work. But in the hands of the FDA, which wants everything, supplements and drugs alike, to go through the vastly expensive new drug approval process, we fear the new rules will be used to forbid the development or sale of any new supplements—where “new” means anything after 1994, when DSHEA was passed.
READ MORE...
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