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OpEdNews Op Eds    H4'ed 5/16/09

Codex Alimentarius and Non-European Countries - Part One

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Part One: A storm is brewing...

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The future of each nation's natural health industry, nutritional innovation and each individual's personal freedom of choice regarding access to a wide range of vitamin supplements, amino acids, herbs and ancient and modern traditional medicines, appears with little doubt to be at genuine risk in the not-too-distant future. One can later speculate and even try to reason the intentions and motivations that have brought about this situation; however, it is certain that the situation exists and is no accident of circumstances.

This article will attempt to explain, document, and clarify the actual situation by separating the facts from numerous assertions, biased interpretations, and short-sighted solutions being attempted.

The situation we face is primarily the result of a series of apparently unrelated, but in fact, well-coordinated and complex events; executed slowly over time in incremental steps. It is a situation driven by vested interests, implemented by cooperating foreign and national governmental representatives, agencies, and legislative bodies, and fully upheld by a number of international trade agreements signed by heads of state.

While much confusion, conflicting opinion, and even heated argument exist as to the legal relevance and potential influence of "Codex Alimentarius" (Codex) to the future of vitamin supplements, herbs, amino acids, and many widely accepted forms of traditional medicines, the story does not begin in the Americas.

It began in the European Union.

In Europe, the European Food Supplement's Directive was legislated and brought into law in 2002. The EU Food Supplements Directive was then upheld in the European Court of Justice despite fierce legal challenges by watchdog organizations within the natural health community in 2005.

These unnecessary and severely restrictive pieces of European legislation are now in various stages of clarification, finalization, and implementation throughout the European Union.

In summary, the EU Food Supplements Directive will:

(a) Eliminate (completely ban) almost two-in-every-three currently available vitamin substances, amino acids, herbs; and traditional medicines;

(b) Dramatically reduce dosage levels to newly established Maximum Permitted Levels (MPLs), based on a severely flawed procedure for assessing risk (no consideration is even given to existing benefits) and directly influenced by pharmaceutical industry participants;

(c) Reclassify the remaining "allowable" vitamin substances as medicine;

(d) Severely censor what the industry itself or any practitioner can promote, publish, or say about their mental or physiological influence.

Amino acids, herbs, Ayurvedic and other long-accepted, traditional health remedies are also under the EU Food Supplements Directive's legislative control.

Natural products and vitamin substances that have not been approved, or those of manufacturers who fail to provide adequate and fully documented dossiers to the authorized governing bodies, will begin to be removed from the shelves in shops and websites throughout Europe in the months to come.

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Lord Rudi C. Loehwing Social Media Pages: Facebook Page       Twitter Page       Linked In Page       Instagram page url on login Profile not filled in

Lord Rudi C. Loehwing (baron), Managing Director for a non-profit campaign organization; the World Institute of Natural Health Sciences, (WINHS.ORG). Producer and narrative director of documentary films, radio and television programs. (more...)

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