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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 …We examine market share and price trends in the quarter century since the 1984 Waxman-Hatch legislation. The generic …. Whereas in 1994 the generic price index fell from 100 to 65 in the 24 months following initial generic entry, in 2009 the …
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By introducing n (>1) firms with infinite cross-price elasticity (i.e. generic drugs), we explore the effects of … the reference price (R) does not depend on the price of the branded product. When generics collude, the way R is designed …
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In order to contain expenditures for pharmaceuticals, the latest healthcare reforms have focused on decentralising …
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