An FDA for Financial Innovation: Applying the Insurable Interest Doctrine to 21st Century Financial Markets

E. Posner, E. Weyl
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引用次数: 79

Abstract

The financial crisis of 2008 was caused in part by speculative investment in complex derivatives. In enacting the Dodd-Frank Act, Congress sought to address the problem of speculative investment, but merely transferred that authority to various agencies, which have not yet found a solution. We propose that when firms invent new financial products, they be forbidden to sell them until they receive approval from a government agency designed along the lines of the FDA, which screens pharmaceutical innovations. The agency would approve financial products if they satisfy a test for social utility that focuses on whether the product will likely be used more often for insurance than for gambling. Other factors may be addressed if the answer is ambiguous. This approach would revive and make quantitatively precise the common-law insurable interest doctrine, which helped control financial gambling before deregulation in the 1990s.
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金融创新的FDA:可保利益原则在21世纪金融市场的应用
2008年金融危机的部分原因是对复杂衍生品的投机性投资。在颁布《多德-弗兰克法案》(Dodd-Frank Act)时,国会试图解决投机性投资的问题,但只是将权力移交给了各个机构,而这些机构尚未找到解决办法。我们建议,当公司发明新的金融产品时,在获得政府机构的批准之前,禁止销售这些产品,该机构的设计思路与FDA类似,后者负责筛选制药创新。如果金融产品满足社会效用测试,该机构将批准该产品,该测试的重点是该产品是否可能更多地用于保险而不是赌博。如果答案模棱两可,其他因素可能会被提及。这种方法将重振普通法上的可保利益原则,并使之在数量上更加精确。在上世纪90年代放松管制之前,普通法上的可保利益原则曾帮助控制金融赌博。
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