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The textbook of pharmaceutical medicine

Author: J P Griffin; John O'Grady, Professor.
Publisher: Oxford ; Malden, Mass. : Blackwell, ©2006.
Edition/Format:   Print book : English : 5th edView all editions and formats
Database:WorldCat
Summary:
Text contains revised chapters on drug regulation in the USA and additional chapters on pharmaco-economics. Topics include discoveries, toxicity testing, clinical trials, development of medicines, and much more.
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Genre/Form: Lehrbuch
Material Type: Internet resource
Document Type: Book, Internet Resource
All Authors / Contributors: J P Griffin; John O'Grady, Professor.
ISBN: 0727918400 9780727918406
OCLC Number: 60543263
Description: x, 870 pages : illustrations ; 25 cm
Contents: Discovery of new medicines / Anand S. Dutta --
Pharmaceutical development / Gavin Halbert --
Preclinical safety testing / David J. Tweats --
Exploratory development / John Posner --
Clinical pharmacokinetics / Paul Rolan and Valeria Molnar --
Purpose and design of clinical trials / Roger A. Yates --
Conduct of clinical trials : good clinical practice / Roger A. Yates --
Medical statistics / Andrew P. Grieve. Development of medicines : full development / Alan G. Davies and Peter D. Stonier --
The medical department / Darrall L. Higson with revisions by Peter D. Stonier --
Medical marketing / John H. Young --
Information and promotion / D. Michael Humphreys --
The supply of unlicensed medicines for particular patient use / Amanda Wearing and John O'Grady --
Legal and ethical issues relating to medicinal products / Christine H. Bendall, Christopher J.S. Hodges --
The safety of medicines / A. Peter Fletcher and Susan Shaw --
History of drug regulation in the United Kingdom / John P. Griffin and Rashmi R. Shah --
Regulation of human medicinal products in the European Union / Rashmi R. Shah and John P. Griffin. European regulation of medicinal devices / Christopher J.S. Hodges --
Technical requirements for registration of pharmaceuticals for human use : the ICH process / Dean W.G. Harron --
The regulation of drug products by the United States food and drug administration --
Peter Barton Hutt --
The US FDA in the drug development, evaluation and approval process / Richard N. Spivey, Judith K. Jones, William Wardell and William Vodra --
Past evolution and future prospects of the Pharma Industry and its regulation in the USA / William Wardell, William Vodra, Judith K. Jones and Richard N. Spivey --
Regulatory and clinical trial approval systems in Japan / Yuichi Kubo --
The regulation of therapeutic products in Australia / Janice Hirshorn and Deborah Monk --
Economics of healthcare / Carole Bradley and Jane R. Griffin --
Controls on NHS medicines prescribing and expenditure in the UK (an historical perspective) with some international comparisons / John P. Griffin and Jane R. Griffin.
Responsibility: edited by John P. Griffin and John O'Grady.
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Abstract:

Text contains revised chapters on drug regulation in the USA and additional chapters on pharmaco-economics. Topics include discoveries, toxicity testing, clinical trials, development of medicines, and much more.

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