© 1996 Oxford University Press
Substitution in Regulatory Agencies: FDA Enforcement Alternatives
Washington University
This article develops a framework to understand the factors to which regulatory agencies respond and examines how these factors may influence agency decision-making. The model shows how either changing feedback from constituents or changing regulatory costs can alter the trade-offs facing the agency and hence create opportunities for substitution among different agency actions. This framework is used to explain the changing portfolio of FDA enforcement actions between 197292. Results indicate that changing constituent and political feedback is the reason for the observed policy change. Specifically, budget reductions and increasing industry demand for product approval led the FDA to reduce monitoring and substitute less resource-intensive enforcement, namely recalls, for more resource-intensive enforcement. Results also show that increasing numbers of adverse drug reaction reports from consumers and physicians enabled the agency to increase the efficiency of its inspections policy and to ultimately reduce its use of inspections.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
J. Paradise, A. W. Tisdale, R. F. Hall, and E. Kokkoli Evaluating Oversight of Human Drugs and Medical Devices: A Case Study of the FDA and Implications for Nanobiotechnology J. Law Med. Ethics, December 1, 2009; 37(4): 598 - 624. [PDF] |
||||
![]() |
S. Gilad Juggling Conflicting Demands: The Case of the UK Financial Ombudsman Service J. Public Adm. Res. Theory., July 1, 2009; 19(3): 661 - 680. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Grant and K. C. Alfred Sanctions and Recidivism: An Evaluation of Physician Discipline by State Medical Boards Journal of Health Politics Policy and Law, October 1, 2007; 32(5): 867 - 885. [Abstract] [PDF] |
||||
![]() |
P. Fenn, A. Gray, and N. Rickman Standard fees for legal aid: an empirical analysis of incentives and contracts Oxf. Econ. Pap., October 1, 2007; 59(4): 662 - 681. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. T. Law How do Regulators Regulate? Enforcement of the Pure Food and Drugs Act, 1907-38 J. Law Econ. Organ., October 1, 2006; 22(2): 459 - 489. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. K. Olson Managing Delegation in the FDA: Reducing Delay in New-Drug Review Journal of Health Politics Policy and Law, June 1, 2004; 29(3): 397 - 430. [Abstract] [PDF] |
||||
![]() |
G. W. Cox The Empirical Content of Rational Choice Theory: A Reply to Green and Shapiro Journal of Theoretical Politics, April 1, 1999; 11(2): 147 - 169. [Abstract] [PDF] |
||||





