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Regulating complementary medicine

机译:调节辅助药物

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The growth of complementary medicine has been accompanied by calls for tighter regulation. These come from three main sources: consumer organisations that are concerned that the existing common law freedom to practise puts the public at risk; complementary therapists, fuelled by fears of European harmonisation and medical "colonisation"; and the medical profession, which is increasingly tolerant towards complementary medicines, provided they can be shown to be safe. Until now in Britain there has been an uncritical assumption that tighter regulation necessarily means statutory regulation along the lines of the Medical Act 1983. Osteopaths and chiropractors have successfully pursued this route, and acupuncturists, homoeopaths, and herbalists may attempt to follow. The Osteopaths Act 1993 and the Chiropractors Act 1994 are significant improvements on the Medical Act 1983. They introduce, for example, a definition of "unacceptable professional conduct" that embraces professional incompetence (the medical profession has also now introduced performance review through the Medical (Professional Performance) Act 1995), as well as requirements for continuous professional development. However, the structure of the legislation is otherwise the same.
机译:伴随着补充医学的增长,人们呼吁加强监管。这些主要来自三个方面:消费者组织,他们担心现有的普通法实践自由会使公众处于危险之中;对欧洲协调和医学“殖民化”的恐惧助长了辅助治疗师;可以证明对补充药物的安全性越来越强的医学界。迄今为止,在英国,一直没有一个严格的假设,即严格的监管必然意味着要按照1983年《医疗法》进行法定监管。整骨医生和脊医已经成功地遵循了这条路线,针灸师,整骨医生和中医师可能会尝试遵循。 《 1993年整骨者法》和《 1994年脊医》是对1983年《医疗法》的重大改进。例如,它们引入了“不可接受的专业行为”的定义,其中包括专业上的无能(医疗行业现在也通过《医疗法》引入了绩效评估( 1995年《专业绩效法》),以及持续专业发展的要求。但是,立法的结构在其他方面是相同的。

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