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Monday, February 04, 2008
Phyllis Schlafly :: Townhall.com Columnist
China Trade: Patents, Poisons, and Prescription Drugs
by Phyllis Schlafly
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Will the Dems' health care Christmas Present to America be an improvement or detriment to our health care system?


That number is increasing as the Chinese government is steadily repatriating its scientists who were trained in the United States. The hai gui, skilled Western-trained Chinese returnees who studied and worked in the U.S. for many years, acquiring academic and commercial experience, are now going back to China to take important positions at salaries that are one-third to one-fifth of U.S. salaries.

An estimated 80 percent of the active pharmaceutical ingredients used to make drugs sold in the United States are imported, and an estimated 40 percent of finished drugs are made in foreign countries. The Chinese drug agency does not even oversee the making of pharmaceutical raw materials, called intermediates, which are the building blocks for active pharmaceutical ingredients.

The U.S. Food and Drug Administration is slated to inspect only 13 of China's 714 drug firms, 1.8 percent, this year. U.S. drugmakers are inspected at least once every two years, but there is no such requirement about imports, and Government Accountability Office spokeswoman Marcia Crosse admitted that 13 years can pass before a foreign manufacturer is visited even once.

The Associated Press reported that when the FDA does visit foreign plants, its inspectors can make "sometimes harrowing findings."

Even when Chinese manufacturers are inspected, our FDA inspectors rely on the companies for translators, and U.S. firms are required to authorize a Chinese official to serve as its legal representative. One U.S. CEO said, "Every piece of information you get is suspect."

At the Cambridge Healthtech Drug Development in China conference in Philadelphia in September, Chinese speakers bragged that China offers opportunities to lower costs for preclinical and clinical drug development activities. The cost of doing preclinical studies and clinical trials in China is about 20 percent to 60 percent of U.S. costs and can be many months faster, so U.S. multinationals follow the money.

But clinical trial applications are risky because there is no well-defined process, and Chinese regulations mean little because everything is ultimately decided on a local level. How can we know that the drugs in our medicine chest are safe?

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About The Author

Phyllis Schlafly is a national leader of the pro-family movement, a nationally syndicated columnist and author of Feminist Fantasies.
 
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MY OWN "CHINA SYNDROME"
I have written of this subject in blog here on the "pages" of Townhall.

On a campaign to boycott everything I can see that's made in China, I have found it difficult to shop at all. One of my blogs is named "Isn't Everything Made in China?"

I have suggested to Von Eschenbach and to my U.S. lawmakers that every product, that every prescription sold here in the U.S., bear labels showing countries of origin of everything making up that product as well as the country of origin of manufacture.

I don't care if a prescription bottle has to be four times bigger, or ten times bigger, I want to know the origin of all the parts of that prescription.

You can't buy a can of mandarin oranges that doesn't come from China; same for pineapple, for heaven's sake. Same for many, many things that have a "distributed by" label bearing the name of a U.S. distributor. Call that distributor; you'll find that much of the time the item originated in China.

I'm sick of it. We all may die from it. The FDA now has a "partnership" with China. Who's going to pay for all this? Americans. I've had it. China can go to you-know-where for all I care. And so can all of its products.

Thanks again to Ms. Schlafly for bringing such important subjects to our attention.


Subs
Japanese subs that operated off the US west coast did so after 12/7/1941 which at that time the US and Japan were at war. Japan made the final decision go to war on 12/1/1941.

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