Updated excerpt from Codex Alimentarius — The End of Health Freedom 

Available Here

Brandon Turbeville
Activist Post

In my last article regarding Codex Alimentarius Guidelines on Genetically Modified food, I discussed the dangerous concept used by both the international organization and the U.S. Food and Drug Administration (FDA) known as substantial equivalence/substantial similarity and how this method of comparison and evaluation can and is being used to further the proliferation of GM food in the world’s food supply.

In discussing the method used to evaluate the safety of GM food, I wrote,

If Codex is willing to accept the safety assessments of regulatory agencies without independent testing of its own and regulatory agencies are willing to accept the safety assessments of corporations without independent testing of their own, then Codex is willing to accept the safety assessments of corporations without independent safety testing of their own. Indeed, this syllogism adequately reflects the reality of the relationship between Codex, corporations, and the future of GM foods.

Furthermore, in regards to the “substantial equivalence” methodology mentioned above, I concluded the article by stating,

Allowing GM products to be compared to other GM products for substantial equivalence is an enormous blow to the environment, human health, and consumer choice. Such an action would completely undercut the already weak and ridiculous method of substantial equivalence and would turn the entire nature of our food supply upside down. One would be comparing a dangerous product to another dangerous product but labeling it safe because it was substantially equivalent to the first dangerous product.

Like the situation involving vitamins and minerals, this is the Twilight Zone reality produced by Codex once it gains power of the food supply.

Unfortunately, this potential concern is now an imminent one because Monsanto has in fact submitted an application for a GM corn called LY038. In its submission for approval, Monsanto provided the regulators’ assessing the product with information comparing LY038 with another GM corn product called LY038 (-), another GM corn product.[1]
True to form, in many of the pro-GM countries such as New Zealand, Australia, Japan, Canada, the Philippines, and South Korea, the LY038 corn was approved based upon the method of using a GM corn as a conventional counterpart.[2] The United States, being the most open to GM food, and only requiring voluntary submission, has also approved LY038 for cultivation.[3]

Thankfully, the Monsanto agenda stalled in the European Union, and in 2009 Monsanto withdrew its application for the product in Europe.[4] This is largely due to a small group of relatively independent scientists from the Centre for Integrated Research in Biosafety (INBI) out of New Zealand who brought out many risks evident from a close reading of the Monsanto application dossiers.

As a result of their work, the European Food Safety Authority (EFSA) requested additional research and safety data. That was all that was needed in order to cause Monsanto to withdraw its application for LY038 use in Europe.[5]

Monsanto claimed that the reason for the removal of its submission purely economical and that “although our preference would have been to complete the EU approval of LY038, conducting further studies, as requested [by the EFSA GMO Panel], can no longer be justified, in view of the additional costs involved and the reduced commercial interest in this product.”[6]

However, those who are aware of Monsanto’s track record have a different take. In a statement made to Biosafety Information Centre, Prof. Jack Heinemann, who led the INBI research team, summed up the situation succinctly.

 

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