Guest guest Posted June 6, 2007 Report Share Posted June 6, 2007 Here is an excellent article by Paul Taylor posted on the Dr. Rath website, which explains how the FDA's officials are co-operating with the European Union's health directorate to bring about a harmonized regulatory environment for supplements between the US and Europe, and why that regulatory environment will be a direct and rather painful limitation to the freedom of choice of US consumers unless - there is a real outcry that can't be overheard... Kind regards Sepp EU-U.S. Summit Signals New Threats To Natural Health Therapies http://www4.dr-rath-foundation.org/us/summit07/index.html .... because the European Food Supplements Directive was used as the blueprint for what is now effectively the global standard for dietary supplement regulations – the Codex Guidelines for Vitamin and Mineral Food Supplements – European regulations are, by definition, already compliant with that standard. As such, it is clear that in order to achieve the goal of transatlantic harmonization, American dietary supplement legislation will have to be harmonized to the restrictive European model, as opposed to the other way around. Given this reality, one should perhaps not be surprised to discover that regulatory cooperation between the FDA and DG SANCO (the European Commission’s Health and Consumer Protection Directorate) is already well advanced. The ultimate aim behind the recent increase in domestically-based attacks on supplements in the U.S. can be seen as being to prepare the ground for the eventual dismantling of DSHEA and the harmonization of the U.S. dietary supplement market to the more restrictive legislative regimes that exist in Europe and - via the planned North American Union – Canada and Mexico. As such, although neither the Codex Guidelines for Vitamin and Mineral Food Supplements – the global standard – or the Food Supplements Directive – the European standard – have as yet set any maximum permitted doses for nutrients contained in supplements, it would seem reasonable to conclude that whatever levels are announced later this year by the European Commission could - as a result of both European political power at Codex meetings and the trans- Atlantic regulatory cooperation outlined above - eventually be exported to, and implemented in, the United States. To see the whole article: http://www4.dr-rath-foundation.org/us/ summit07/index.html Quote Link to comment Share on other sites More sharing options...
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