Protection without Capture: Product Approval by a Politically Responsive, Learning Regulator
When policy arrangements appear to favor well-organized and wealthy interests, should we infer “capture” of the political process? In particular, might larger firms receive regulatory “protection” even when the regulatory agency is not captured by producers? I model regulatory approval—product appro...
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Veröffentlicht in: | The American political science review 2004-11, Vol.98 (4), p.613-631 |
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description | When policy arrangements appear to favor well-organized and wealthy interests, should we infer “capture” of the political process? In particular, might larger firms receive regulatory “protection” even when the regulatory agency is not captured by producers? I model regulatory approval—product approval, licensing, permitting and grant making—as a repeated optimal stopping problem faced by a learning regulator subject to variable political pressure. The model is general but stylistically applied to pharmaceutical regulation. Under the assumption that consumers are differentially organized, but producers are not, there nonetheless exist two forms of “protection” for larger, older producers. First, firms submitting more applications may expect quicker and more likely approvals, even in cases where their reputations for safety are below industry average. Second, “early entrants” to an exclusive market niche (disease) receive shorter expected approval times than later entrants, even when later entrants offer known quality improvements. The findings extend to cases of bounded rationality and a reduced form of endogenous firm submissions. The model shows that even interest-neutral “consumer” regulation can generate protectionist outcomes, and that commonly adduced evidence for capture is often observationally equivalent to evidence for other models of regulation. |
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In particular, might larger firms receive regulatory “protection” even when the regulatory agency is not captured by producers? I model regulatory approval—product approval, licensing, permitting and grant making—as a repeated optimal stopping problem faced by a learning regulator subject to variable political pressure. The model is general but stylistically applied to pharmaceutical regulation. Under the assumption that consumers are differentially organized, but producers are not, there nonetheless exist two forms of “protection” for larger, older producers. First, firms submitting more applications may expect quicker and more likely approvals, even in cases where their reputations for safety are below industry average. Second, “early entrants” to an exclusive market niche (disease) receive shorter expected approval times than later entrants, even when later entrants offer known quality improvements. The findings extend to cases of bounded rationality and a reduced form of endogenous firm submissions. 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In particular, might larger firms receive regulatory “protection” even when the regulatory agency is not captured by producers? I model regulatory approval—product approval, licensing, permitting and grant making—as a repeated optimal stopping problem faced by a learning regulator subject to variable political pressure. The model is general but stylistically applied to pharmaceutical regulation. Under the assumption that consumers are differentially organized, but producers are not, there nonetheless exist two forms of “protection” for larger, older producers. First, firms submitting more applications may expect quicker and more likely approvals, even in cases where their reputations for safety are below industry average. Second, “early entrants” to an exclusive market niche (disease) receive shorter expected approval times than later entrants, even when later entrants offer known quality improvements. The findings extend to cases of bounded rationality and a reduced form of endogenous firm submissions. The model shows that even interest-neutral “consumer” regulation can generate protectionist outcomes, and that commonly adduced evidence for capture is often observationally equivalent to evidence for other models of regulation.</description><subject>Administrative agencies</subject><subject>Approval</subject><subject>Capital costs</subject><subject>Commercial regulation</subject><subject>Competition</subject><subject>Consumers</subject><subject>Drug design</subject><subject>Drug regulation</subject><subject>Economic regulation</subject><subject>Enterprises</subject><subject>Evidence</subject><subject>Familiarity</subject><subject>FDA approval</subject><subject>Financial regulation</subject><subject>Government (Administrative Body)</subject><subject>Government Policy</subject><subject>Government Regulation</subject><subject>Industrial regulation</subject><subject>Inferences</subject><subject>Litigation</subject><subject>Medicine</subject><subject>Pharmaceutical industry</subject><subject>Pharmaceutical preparations</subject><subject>Political economy</subject><subject>Political Influences</subject><subject>Political science</subject><subject>Politics</subject><subject>Prescription drugs</subject><subject>Product lines</subject><subject>Product quality</subject><subject>Product safety</subject><subject>Products</subject><subject>Protectionism</subject><subject>Regulated industries</subject><subject>Regulation</subject><subject>Regulatory approval</subject><subject>Regulatory 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without Capture: Product Approval by a Politically Responsive, Learning Regulator</title><author>CARPENTER, DANIEL P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c485t-7d1f1eddf688a33e5f54d837ac2498bb12a46d333b38bc9a95db8e73995fd0d33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Administrative agencies</topic><topic>Approval</topic><topic>Capital costs</topic><topic>Commercial regulation</topic><topic>Competition</topic><topic>Consumers</topic><topic>Drug design</topic><topic>Drug regulation</topic><topic>Economic regulation</topic><topic>Enterprises</topic><topic>Evidence</topic><topic>Familiarity</topic><topic>FDA approval</topic><topic>Financial regulation</topic><topic>Government (Administrative Body)</topic><topic>Government Policy</topic><topic>Government Regulation</topic><topic>Industrial regulation</topic><topic>Inferences</topic><topic>Litigation</topic><topic>Medicine</topic><topic>Pharmaceutical industry</topic><topic>Pharmaceutical preparations</topic><topic>Political economy</topic><topic>Political Influences</topic><topic>Political science</topic><topic>Politics</topic><topic>Prescription drugs</topic><topic>Product lines</topic><topic>Product quality</topic><topic>Product safety</topic><topic>Products</topic><topic>Protectionism</topic><topic>Regulated industries</topic><topic>Regulation</topic><topic>Regulatory approval</topic><topic>Regulatory theory</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CARPENTER, DANIEL P.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>ProQuest Social Sciences Premium Collection</collection><collection>ProQuest Central (Corporate)</collection><collection>Worldwide Political Science Abstracts</collection><collection>Access 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Rev</addtitle><date>2004-11-01</date><risdate>2004</risdate><volume>98</volume><issue>4</issue><spage>613</spage><epage>631</epage><pages>613-631</pages><issn>0003-0554</issn><eissn>1537-5943</eissn><coden>APORBP</coden><abstract>When policy arrangements appear to favor well-organized and wealthy interests, should we infer “capture” of the political process? In particular, might larger firms receive regulatory “protection” even when the regulatory agency is not captured by producers? I model regulatory approval—product approval, licensing, permitting and grant making—as a repeated optimal stopping problem faced by a learning regulator subject to variable political pressure. The model is general but stylistically applied to pharmaceutical regulation. Under the assumption that consumers are differentially organized, but producers are not, there nonetheless exist two forms of “protection” for larger, older producers. First, firms submitting more applications may expect quicker and more likely approvals, even in cases where their reputations for safety are below industry average. Second, “early entrants” to an exclusive market niche (disease) receive shorter expected approval times than later entrants, even when later entrants offer known quality improvements. The findings extend to cases of bounded rationality and a reduced form of endogenous firm submissions. The model shows that even interest-neutral “consumer” regulation can generate protectionist outcomes, and that commonly adduced evidence for capture is often observationally equivalent to evidence for other models of regulation.</abstract><cop>New York, USA</cop><pub>Cambridge University Press</pub><doi>10.1017/S0003055404041383</doi><tpages>19</tpages></addata></record> |
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subjects | Administrative agencies Approval Capital costs Commercial regulation Competition Consumers Drug design Drug regulation Economic regulation Enterprises Evidence Familiarity FDA approval Financial regulation Government (Administrative Body) Government Policy Government Regulation Industrial regulation Inferences Litigation Medicine Pharmaceutical industry Pharmaceutical preparations Political economy Political Influences Political science Politics Prescription drugs Product lines Product quality Product safety Products Protectionism Regulated industries Regulation Regulatory approval Regulatory theory Studies |
title | Protection without Capture: Product Approval by a Politically Responsive, Learning Regulator |
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