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Essay / Research Paper Abstract
This 4 page paper provides an overview of two aspects effecting global competition in health care: stem cell research and telemedicine. This paper considers their implications in relation to international competition. Bibliography lists 7 sources.
Page Count:
4 pages (~225 words per page)
File: MH11_MHsteceint.doc
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to maintain their status as a top producer of medical research, especially in areas like stem cell research that has considerable promise, while also preventing breaches of ethics. Maintaining
a global competitive edge in research requires a careful balance between medically necessary research areas and ethically suspect research. National debates over stem cell research, for example, have led
to questions about regulatory control and international competition. Stem Cell Research Debates over the international focus on stem cell research have altered perspectives on the use
of specific types of research. The Bush Administration sought an international ban on all cloning of human cells, including reproductive cloning and cloning used to produce stem cells (embryonic
cloning) (Herold & Daley, 2007). Though the Bush Administration finally pulled back from an effort to have both types of cloning banned at an international level, bans were placed
on the use of embryonic tissues in both research and medical practices. Scientific research involving human genetic research has led to national, European, and international regulatory controls, that relate
to the ethics of human research and the need to ensure protections against human cloning. While international governing bodies have struggled to define applicable international laws about human reproductive
and scientific research, general regulations prohibiting the cloning of humans for reproductive purposes have been applied internationally. Developing protocols for embryonic stem cell research has required governing bodies to
consider the nature of human research within the scope of limits regarding reproductive experimentation. "There are also numerous non-binding international declarations, guidelines and other soft-law documents that deal with scientific
research, genetics, human reproduction, etc." that limit approaches to research when human genetic materials are involved (Taupitz, 2010, p. 215). If regulatory control in the United States is
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