The textbook of pharmaceutical medicine /

Bibliographic Details
Other Authors: Griffin, J. P. (John Parry), O'Grady, John, Professor
Format: eBook
Language:English
Published: Oxford ; Malden, Mass. : Blackwell, [2006]
Edition:5th ed.
Series:Wiley Online Library.
Subjects:
Online Access:Connect to the full text of this electronic book

MARC

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245 0 4 |a The textbook of pharmaceutical medicine /  |c edited by John P. Griffin and John O'Grady. 
250 |a 5th ed. 
264 1 |a Oxford ;  |a Malden, Mass. :  |b Blackwell,  |c [2006] 
264 4 |c ©2006 
300 |a 1 online resource (x, 870 pages) :  |b illustrations 
336 |a text  |b txt  |2 rdacontent 
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500 |a Electronic resource. 
504 |a Includes bibliographical references and index. 
505 0 |a 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. 
505 0 |a 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. 
588 |a Description based on print version record. 
650 1 2 |a Drug Approval.  |0 https://id.nlm.nih.gov/mesh/D017277 
650 2 2 |a Clinical Trials as Topic.  |0 https://id.nlm.nih.gov/mesh/D002986 
650 2 2 |a Pharmacology.  |0 https://id.nlm.nih.gov/mesh/D010600 
650 0 |a Pharmacology, Experimental.  |0 http://id.loc.gov/authorities/subjects/sh85100600 
650 6 |a Pharmacologie expérimentale. 
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