Posted on 03/18/2006 7:38:52 PM PST by hedgetrimmer
The debate over the National Uniformity for Food Act is heating up following hearings in Washington, D.C., last week.
Congress debated the pros and cons of H.R. 4167, which proponents claim will eliminate differences in food safety laws between states, simplify requirements for manufacturers, and help facilitate intrastate commerce.
The bill was introduced in October of 2005, but due to the controversial nature of its contents, has not received universal support.
Opponents see the bill as hindering states' abilities as first responders and pre-empting state laws like California's Prop. 65, which requires food warning labels to notify consumers of toxic contents in consumer products.
This includes warnings regarding mercury in fish, arsenic in water, and lead content in candy imported from Mexico.
According to a statement in a press release from Rep. Anna Eshoo (D-CA), "Under this bill (H.R. 4167), the FDA [Food and Drug Administration] will have to approve any food safety law that is at variance with federal policy."
Eshoo has also voiced concern over funding needed to implement such an extensive undertaking, saying it would cost the FDA $100 million over the next 5 years to process petitions from states seeking to retain their laws.
Approval of H.R. 4167 seems elusive since support is divided along partisan lines. Republicans, who usually support state's rights over big government, are generally in favor of adding more FDA regulation and giving the federal government more control. Democrats, who usually support federal regulations, are generally opposing the bill and supporting states' rights to determine their own laws.
The bill also raises serious questions about public safety and national security regarding food tampering and terrorism. Both sides argue that their position would help protect the U.S. from foreign or domestic tampering and provide the best response to terrorism.
This is an outgrowth of the WTO. You'll note it isn't being billed that way - on purpose.
The source, my friend, is everything.
I didn't even read the article. Why would I read another alarmist story if I knew the source to specialize in such stories, to some end known only to them?
The source is at least as important as what is contained in the article, because the article isn't immediately verifiable in its content or implications, at least to the vast majority of the readers. the objectivity and/or bias, and any agenda of the source is key.
as to the paper itself, I found it to be very articulate, aimed at something higher than current 8th grade reading skills. It sourced AP and UPI for most of its major content -- that is red flag two. Red flag one is the fact that it's free in New York City, and boasts itself to be an essential, objective organ.
The Falun Gong, themselves have a good story. Beatings and banning by the evil Red Chinese government, etc. How bad can they be? On the other hand, they have lots of angles. They're peddling cheesy and tasteless 9/11 trinkets, t-shirts, pictures and holograms all around Ground Zero. They harangue Wall Street tourists with thier tales of woe. The meditate publicly and animatedly. They obviously have a good PR department, because they're calculatingly efficient in their PR and fundraising efforts.
Seems any reasonable observer would ask himself, "what's this hustle about?"
It does neither. It concentrates markets into oligopoly that eventually raises prices and protects against new entrants and market substitutes by economies of scale and power to influence the regulatory process, but that's not on your list of soundbites.
The cost of compliance is staggering but that's the fault of Congress and those in the public who should be referred to as toxic terrorists. There is no love between the FDA, big pharma, small pharma and the food industry. To claim otherwise means you don't understand either industry but like to pretend you do.
While those within the industry may complain about it, the OWNERS of big pharma want it that way in a similar manner to virtually every other heavily regulated market.
The owners of pharmaceutical companies are the shareholders. As a shareholder, I'd like the FDA to ease their regulations and allow the drug companies to take more risk. If you look at the returns of pharmaceutical stocks in recent history you'll find that the FDA hasn't been providing them much help as most drug company performance has been seriously lacking.
You also claim that competition is limited. If you understood the industry at all you'd know that small start ups and individual entrepreneurs, who have discovered new technologies and treatments, are being made instant millionaires by the drug companies by buying their technology and research.
I suspect you're just another one who believes that all business, especially if it's big, is somehow evil and colluding with government to stick it to the people. As with all folks who believe this kind of crap, they never really know what they're talking about.
Hedge, you never cease to amaze me with the breadth of your knowledge, training and experience. So now you're an expert in biochemistry and physiology. Ok then, explain to me exactly how these maladies occur because of the evil fructose. I'd be very interested in your take on the subject and your ability to separate legitimate research from the junk science out there that is designed and undertaken to create more research dollars.
Wow me with your grasp of biochemistry. Feel free to get as technical as you'd like. Maybe you can explain, in your own words, why fructose is solely responsible for these afflictions. Please don't link me to research by others. I'm mostly interested in your understanding of the issue. Unless, of course, you're just another one here who believes things that they can't explain because they really don't understand.
Sorry, but your blind assumptions are insubstantiable. I was a research and development engineer in the medical device business, where the FDA was but one of my regulatory customers. In that position, not only did I invent products for a Fortune 200 company (Becton Dickinson), I wrote the ISO-9001 cmpliant design control system for the subsidiary they sold as well. I have qualified products both in the US, Canada, and the EU, and also obtained environmental permits abroad.
You can learn more about these corrupt mechanics by studying how they work in other markets. I wrote a whole book on their use in environmental regulation. Here is a post about how it works in the electrical power generating business. The game is old, huge, and not well understood.
And why not? I just did because these are people who did research on the subject.
However, one can pick up a book on the Atkins diet and see in simpler words some of what the link is all about.
You know, over the last couple of years I've noticed more 'loudmouths' with join dates of recent vintage trying to squelch all discussion on certain topics--especially those relating to limiting expansions of Federal power. Just an interesting trend I've been noticing.
I have a direct interest in making regulatory government unnecessary and make no bones about it, although I've never made a profit off the effort. My patent application has been in the USPTO for four years without a first office action.
...and keep citing the "Epoch Times." It keeps the standards on FR high.
Actually, what I was doing was refuting your mischaracterization of my post. If you stop now, there will be no need for me to post to this thread again.
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