This paper discusses the laws concerning the export of non-approved drugs by U.S. manufacturers to European countries: Food and Drug Act, industry background, business issues, ethics, need for reform, global regulations and future.
Written in 1995; 4,500 words; 30 sources; $ 135.95
From the Paper:
"This paper will discuss some aspects of the laws concerning the export of non-approved drugs by U.S. manufacturers to European countries. The first part will provide a brief background to the issue, describing the development of the modern pharmaceutical industry and exports. The second part of the paper will discuss some of the most important business issue involved in the export of drugs. The third part of the paper will consider some of the important ethical issues concerning the export of drugs. The fourth part of the paper will examine the U.S. laws and international agreements governing the export of drugs developed in the U.S. The conclusion will consider the future of drug exports and some possible approaches to the problems."
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