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1 [i] (1981)

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The International Supply of Medicines: Implications of U.S. Regulatory
Reforms, edited by Robert B. Helms, presents the proceedings of a
conference, sponsored by AEI's Center for Health Policy Research, on
the international aspects of the reform of the U.S. drug laws. The
papers and commentaries are organized into three parts:
  *  Part One-The  Multinational Pharmaceutical Industry: Evidence
of Product Diffusion and Technology Transfer, contains papers by
Professor Henry G. Grabowski, on the effects of regulation on the
introduction of new drugs in international markets, and by Professor
Josef C. Brada, on economic and regulatory factors affecting pharma-
ceutical research, production, and marketing in international markets.
  *  Part Two-U.S. Regulatory and Patent Reform, contains papers
by Professor Edmund W. Kitch, analyzing how patent and trade-secret
systems affect a firm's management of the research process, and by
Professors Kenneth W. Clarkson, David L. Ladd, and William MacLeod,
analyzing various proposals to release trade secrets.
  *  Part Three-Medicines for the Third World offers a report by
Professor John E. S. Parker on the diffusion of new drugs to Third
World countries and price competition in these markets.
Critical commentaries are provided on each of the papers by experts
from government, the academic community, and the pharmaceutical
industry.


ISBN 0-8447-2190-5 cloth bound edition
ISBN 0-8447-2191-3 paperback edition


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American Enterprise Institute for Public Policy Research
1150 Seventeenth Street, N.W., Washington, D.C. 20036


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         The International


      Supply of Medicines

Implications of U.S. Regulatory Reform


                 Edited by Robert B. Helms

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