Assessing the Safety and Efficacy of the FDA: The Case of the Prescription Drug User Fee Acts
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- Philipson, Tomas J. & Berndt, Ernst R. & Gottschalk, Adrian H. B. & Strobeck, Matthew W., 2005. "Assessing the Safety and Efficacy of the FDA: The Case of the Prescription Drug User Fee Acts," Working Papers 199, The University of Chicago Booth School of Business, George J. Stigler Center for the Study of the Economy and the State.
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Cited by:
- Daniel B. Klein, 2008. "Colleagues, Where Is the Market Failure? Economists on the FDA," Econ Journal Watch, Econ Journal Watch, vol. 5(3), pages 316-348, September.
- Allan Begosh & John Goldsmith & Ed Hass & Randall W. Lutter & Clark Nardinelli & John A. Vernon, 2006. "Black Box Warnings and Drug Safety: Examining the Determinants and Timing of FDA Warning Labels," NBER Working Papers 12803, National Bureau of Economic Research, Inc.
- Vernon, John A. & Golec, Joseph H. & Lutter, Randall & Nardinelli, Clark, 2009. "An exploratory study of FDA new drug review times, prescription drug user fee acts, and R&D spending," The Quarterly Review of Economics and Finance, Elsevier, vol. 49(4), pages 1260-1274, November.
- Olson, Mary K., 2008. "The risk we bear: The effects of review speed and industry user fees on new drug safety," Journal of Health Economics, Elsevier, vol. 27(2), pages 175-200, March.
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This paper has been announced in the following NEP Reports:- NEP-HEA-2005-11-05 (Health Economics)
- NEP-PBE-2005-11-05 (Public Economics)
- NEP-REG-2005-11-05 (Regulation)
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