License to Deal: Mandatory Approval of Complex Financial Products

S. Omarova
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引用次数: 25

Abstract

In the wake of the recent crisis, policy-makers and academics continue to debate how to control and reduce systemic risk associated with financial innovation, complexity, and growing interconnectedness of global financial markets. This Article argues that an effective method of achieving that goal is to establish ex ante regulatory controls that target risk before it is introduced into the financial system. The Article offers the first comprehensive analysis of one particular method of such ex ante regulation – mandatory pre-market product approval – and its potential applicability to complex financial instruments, including derivatives, asset-backed securities, and other structured products.The Article examines key features of three historical experiments with product approval regulation: licensing of pharmaceutical drugs by the U.S. Food and Drug Administration, the European Union’s newly adopted Regulation on Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), and a system of mandatory pre-approval of commodity futures contracts administered by the Commodity Futures Trading Commission from 1974 to 2000. Building on these examples, the Article discusses whether, and how, a similar regime can operate as a gatekeeping device that aims explicitly at reduction of systemic risk and strategic complexity in financial markets. The core of the proposal advanced in this Article is the process for product approval, which would require financial institutions to make an affirmative showing that each complex financial product they intend to market meets three statutory tests: (1) an “economic purpose” test, which would place the burden of proving commercial utility of each proposed financial instrument on the financial institutions seeking approval; (2) an “institutional capacity” test, which would require a review of the applicant firm’s ability to manage the risks and monitor the market dynamics of the proposed product effectively; and (3) a broad “systemic effects” test, which would require a finding that approval of the proposed product does not pose an unacceptable risk of increasing systemic vulnerability and otherwise does not raise significant public policy concerns. The proposed approach does not seek to prohibit any financial activities. It merely imposes the duty to provide information necessary for evaluating potential risks and benefits of a specific financial product on the party that has the best access to such information and the greatest incentives not to disclose it voluntarily. Acknowledging significant implementation challenges, the Article argues that mandatory product approval should be taken very seriously as a potentially effective method of advancing the public interest in the more robust systemic risk prevention, as well as enhancing the efficient operation of financial markets.
交易许可:复杂金融产品的强制性批准
在最近的危机之后,政策制定者和学者继续讨论如何控制和减少与金融创新、复杂性和全球金融市场日益紧密的相互联系相关的系统性风险。本文认为,实现这一目标的有效方法是在风险引入金融体系之前建立针对风险的事前监管控制。本文首次全面分析了这种事前监管的一种特定方法——强制性上市前产品批准——及其对复杂金融工具(包括衍生品、资产支持证券和其他结构性产品)的潜在适用性。本文考察了产品审批监管的三个历史实验的主要特征:美国食品和药物管理局对药品的许可,欧盟新采用的化学品注册、评估、授权和限制条例(REACH),以及1974年至2000年由商品期货交易委员会管理的商品期货合同的强制性预先批准制度。在这些例子的基础上,本文讨论了一个类似的制度是否以及如何作为一个明确旨在降低金融市场系统性风险和战略复杂性的把关装置来运作。本文提出的提案的核心是产品审批流程,这将要求金融机构做出肯定的证明,表明它们打算销售的每一种复杂金融产品都符合三项法定测试:(1)“经济目的”测试,这将使寻求批准的金融机构承担证明每一项拟议金融工具的商业效用的责任;(2)“机构能力”测试,要求审查申请公司有效管理风险和监测拟议产品市场动态的能力;(3)广泛的“系统效应”测试,这将要求发现批准拟议的产品不会造成增加系统脆弱性的不可接受的风险,否则不会引起重大的公共政策担忧。拟议的办法并不寻求禁止任何金融活动。它只是将提供评估特定金融产品的潜在风险和收益所需信息的义务强加给了最能获得此类信息并有最大动机不自愿披露这些信息的一方。承认重大的实施挑战,文章认为强制性产品批准应该非常认真地对待,作为一种潜在的有效方法,在更强大的系统性风险预防中促进公众利益,并提高金融市场的有效运作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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