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In this paper, the authors document the complex issues facing the FDA in assessing the quality of generic drugs. They conclude that increased transparency as well as the updating of FDA bioequivalence standards may be important to overcome some of these challenges.
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Drug Policy of 1986
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find that once one incorporates substitution to lower priced generics following patent expiration, average price per …
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By introducing n (1) firms with infinite cross-price elasticity (i.e. generic drugs), we explore the effects of competition on the optimal pricing strategies under a Reference Pricing Scheme (RPS). A two-stage model repeated infinite number of times is presented. When stage 1 is competitive, the...
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In order to contain expenditures for pharmaceuticals, the latest healthcare reforms have focused on decentralising …
Persistent link: https://www.econbiz.de/10010670125
This paper looks at the effects of WTO/TRIPS and pharmaceuticals on women. The focus is on the poor and women. The … benefits of health and modern pharmaceuticals. Access to generic low-priced medicines – including medicines for HIV AIDS …
Persistent link: https://www.econbiz.de/10005699276
This paper demonstrates how, by introducing a generic version of its previously-patented product, a branded firm can influence the equilibrium in the generic segment of the market for the product. This in turn can increase the firm’s profits from selling the branded version. We then use...
Persistent link: https://www.econbiz.de/10005230146
directly related to marketing expenditure. Changes in market structure due to patent expiration or other factors is likely to … sold during the period 2000–2004 to analyze the impact of changes in market structure (primarily resulting from patent … exactly offset one another, so the net effect of patent expiration on drug utilization is zero. …
Persistent link: https://www.econbiz.de/10010576130