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来源类型Working Paper
规范类型论文
The Effects of Product Liability Exemption in the Presence of the FDA
Tomas J. Philipson; Eric C. Sun; Dana Goldman
发表日期2009-12-15
出版年2009
语种英语
摘要In the United States, drugs are jointly regulated by the US Food and Drug Administration, which oversees premarket clinical trials designed to ensure drug safety and efficacy, and the liability system, which allows patients to sue manufacturers for unsafe drugs. In this paper, we examine the potential welfare effects of this dual system to ensure the safety of medical products, and conclude that product liability exemptions for FDA regulated activities could raise economic efficiency. When the safety level mandated by the FDA is binding–in the sense that manufacturers will not conduct additional clinical testing beyond what is mandated by FDA–then product liability may reduce efficiency by raising prices without pushing firms, who are already bound by the FDA’s requirements, to invest further in product safety. We consider as a case study the National Vaccine Injury Compensation Program, which sharply reduced vaccine manufacturer’s liability in 1988. We find evidence that the program reduced prices without affecting vaccine safety, suggest that liability limits can enhance economic efficiency in the presence of the FDA. Click here to read the full report as an Adobe Acrobat PDF. Tomas J. Philipson is a visiting scholar at AEI. Dana Goldman is in the School Policy, Planning and Development at the University of Southern California. Eric C. Sun is at the University of Chicago.
主题Health Care
标签FDA ; liability
URLhttps://www.aei.org/research-products/working-paper/the-effects-of-product-liability-exemption-in-the-presence-of-the-fda/
来源智库American Enterprise Institute (United States)
资源类型智库出版物
条目标识符http://119.78.100.153/handle/2XGU8XDN/207044
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Tomas J. Philipson,Eric C. Sun,Dana Goldman. The Effects of Product Liability Exemption in the Presence of the FDA. 2009.
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