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Synopsis
This book is the first to offer a comprehensive examination of the pharmaceutical industry by following the tortuous course of a new drug as it progresses from early development to final delivery. Richard Epstein looks closely at the regulatory framework that surrounds all aspects of making pharmaceutical products today, and he assesses which current legal and regulatory practices make sense and which have gone awry. While critics of pharmaceutical companies call for ever more stringent controls on virtually every aspect of drug development and approval, Epstein cautions that the effect of such an approach will be to stifle pharmaceutical innovation and slow the delivery of beneficial treatments to the patients who need them. The author considers an array of challenges that confront the industry, conflicts of interest among government, academe, and the drug companies; intellectual property rights that govern patents; FDA regulation; pricing disputes; marketing practices; and liability issues, including those brought to light in the recent VIOXX case. Epstein argues that to ensure the continuing creativity, efficiency, and success of the pharmaceutical industry, the best system will feature strong property rights and clearly enforceable contracts, with minimal regulatory and judicial interference.
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About the Author
Richard A. Epstein is James Parker Hall Distinguished Service Professor of Law, University of Chicago, and Peter and Kirstin Bedford Senior Fellow at the Hoover Institution.
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Overdose: How Excessive Government Regulation Stifles Pharmaceutical Innovation
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Yale University Press (edition 1), 2006
ISBN 10: 0300116640
ISBN 13: 9780300116649
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Overdose: How Excessive Government Regulation Stifles Pharmaceutical Innovation
Published by
Yale University Press (edition 1), 2006
ISBN 10: 0300116640
ISBN 13: 9780300116649
Used
Hardcover
Seller: BooksRun, Philadelphia, PA, U.S.A.
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Overdose: How Excessive Government Regulation Stifles Pharmaceutical Innovation
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Overdose: How Excessive Government Regulation Stifles Pharmaceutical Innovation
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Hardback. Condition: Very Good. Offers a comprehensive examination of the pharmaceutical industry by following the tortuous course of a new drug as it progresses from early development to final delivery. This book looks at the regulatory framework that surrounds aspects of making pharmaceutical products and assesses which legal and regulatory practices make sense. Seller Inventory # CIN0300116640VG
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