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Deadly Discounts: How Reimportation Jeopardizes the Safety of the U.S. Pharmaceutical Drug Supply under the Federal Trade Commission Amendment

机译:致命折扣:根据联邦贸易委员会修正案,再进口如何危害美国药品供应的安全

摘要

The amendment to a Federal Trade Commission (FTC) reauthorization bill, previously introduced as Senate Bill 334 (S.334) Pharmaceutical Market Access and Drug Safety Act of 2005 allows for the reimportation of prescription drugs into the United States from approximately 25 countries, including Canada via Internet pharmacies. There are no guarantees that the internet websites advertising as Canadian pharmacies are legitimate. The shipping of pharmaceutical drugs occurs through importation, which refers to drugs produced abroad then later shipped to the U.S., or re-importation, a term applied when drugs are produced in the U.S. and exported for sale to foreign countries and later imported back into the U.S.The amendment attempts to open the border doors even further by allowing increased importation of medicine and requires pharmacies and drug wholesalers to register with the FDA. The potential importers will be subject to frequent, random inspection; however, these inspections are inadequate and more must be done. Some real solutions include electronic pedigrees and authentication technologies. Also, technology must be rotated so that illegitimate manufacturers can not adapt and overcome anti-counterfeiting measures.
机译:联邦贸易委员会(FTC)重新授权法案的修正案(先前称为2005年参议院法案334(S.334))通过了《药品市场准入和药品安全法》,允许从大约25个国家/地区向美国重新进口处方药通过互联网药店在加拿大。不能保证以加拿大药房做广告的互联网网站是合法的。药品的运输是通过进口进行的,进口是指在国外生产,然后再运到美国或再进口的药品,这是指在美国生产药品并出口到国外销售,然后再进口回国的药品。美国该修正案试图通过允许增加药品进口来进一步打开边界之门,并要求药房和药品批发商向FDA注册。潜在的进口商将受到频繁,随机的检查;但是,这些检查是不充分的,必须做更多的工作。一些实际的解决方案包括电子谱系和认证技术。另外,必须对技术进行轮换,以使非法制造商无法适应和克服防伪措施。

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    Bates Nicole C.;

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