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MARC Record from Library of Congress

Record ID marc_loc_2016/BooksAll.2016.part32.utf8:135321938:3472
Source Library of Congress
Download Link /show-records/marc_loc_2016/BooksAll.2016.part32.utf8:135321938:3472?format=raw

LEADER: 03472cam a22003854a 4500
001 2005015284
003 DLC
005 20130531102025.0
008 050526s2006 enka b 001 0 eng
010 $a 2005015284
016 7 $a101248860$2DNLM
020 $a0727918400 (hardback)
020 $a9780727918406$c(hardback)
035 $a(OCoLC)ocm60543263
040 $aDNLM/DLC$cDLC$dNLM$dBWKUK$dBAKER$dOCLCQ$dIXA$dDLC
042 $apcc
050 00 $aRM301.25$b.T49 2006
082 00 $a615/.1$222
245 04 $aThe textbook of pharmaceutical medicine /$cedited by John P. Griffin and John O'Grady.
250 $a5th ed.
260 $aOxford ;$aMalden, Mass. :$bBlackwell,$cc2006.
300 $ax, 870 p. :$bill. ;$c25 cm.
504 $aIncludes bibliographical references and index.
505 0 $aDiscovery 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 --
505 0 $aDevelopment 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 $aEuropean 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.
650 0 $aPharmacology, Experimental.
650 12 $aDrug Approval.
650 22 $aClinical Trials.
650 22 $aPharmacology.
700 1 $aGriffin, J. P.$q(John Parry)
700 1 $aO'Grady, John$c(Professor)
856 41 $3Table of contents$uhttp://www.loc.gov/catdir/toc/ecip0513/2005015284.html
856 42 $3Contributor biographical information$uhttp://www.loc.gov/catdir/enhancements/fy0827/2005015284-b.html
856 42 $3Publisher description$uhttp://www.loc.gov/catdir/enhancements/fy0827/2005015284-d.html