医疗器械发展的责任和后果。

J M Price
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引用次数: 0

摘要

在过去的40年里,医疗产品责任诉讼的大量增加导致了针对药品和设备制造商的大量诉讼。医疗技术和化工行业是产品责任诉讼的主要对象。医生和其他卫生保健提供者愿意接受与使用医疗产品相关的合理程度的风险,与该产品所能实现的效益相比,但普通陪审团不太可能容忍可接受的故障率的概念。原告律师认为,医疗产品行业应遵守绝对责任标准,任何受到医疗产品伤害的人都有权获得赔偿,而不考虑具体情况。高额的赔偿和惩罚性损害赔偿、高昂的保险成本、高昂的辩护成本以及低利润率迫使一些公司将其产品从市场上撤下。医疗或生物材料制造商可以通过采用成功的产品安全计划来显著减少其产品责任的风险。制造商通过适当的设计、测试、制造、标签和销售优质产品,对其产品的质量、安全性和可靠性有重要的控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The liabilities and consequences of medical device development.

A large increase in medical products liability litigation during the past 40 years has resulted in a flood of litigation against drug and device manufacturers. The medical technology and chemical industries are prime targets for products liability litigation. Physicians and other health care providers are willing to accept a reasonable degree of risk associated with the use of a medical product when compared to the benefit to be achieved by that product but lay juries are less likely to tolerate the concept of an acceptable failure rate. Plaintiffs' lawyers believe that the medical products industry should be held to a standard of absolute liability and that anyone injured by a medical product is entitled to recover without regard for the circumstances. Large compensatory and punitive damage awards, the high cost of insurance, large defense costs, and low profit margins have forced some companies to remove their products from the market. The medical or biomaterials manufacturer can significantly reduce its exposure for products liability by adopting a successful product safety program. Manufacturers have significant control over the quality, safety, and reliability of their products through appropriate design, testing, manufacture, labeling, and sale of quality products.

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