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2000
Volume 10, Issue 18
  • ISSN: 1568-0266
  • E-ISSN: 1873-4294

Abstract

Congress carefully crafted the Hatch-Waxman Act to address two competing goals: to spur new pharmaceutical development and to encourage greater public access to generic drugs. To that end, the Act contains important provisions directed to fulfilling each goal, including provisions favorable to either branded drug or generic drug manufacturers. This article addresses those provisions in the context of issues pertaining to patent rights and in light of the congressional goals.

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/content/journals/ctmc/10.2174/156802610793176666
2010-12-01
2025-09-15
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