000 | 03528nam a22004094a 4500 | ||
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001 | 0000101553 | ||
005 | 20171002055251.0 | ||
006 | m u | ||
007 | cr cn||||||||| | ||
008 | 050526s2006 enka sb 001 0 eng | ||
010 | _z 2005015284 | ||
016 | 7 |
_z101248860 _2DNLM |
|
020 | _z9780470987261 | ||
020 | _z0727918400 (hardback) | ||
020 | _z9780727918406 | ||
035 | _a(CaPaEBR)ebr10236712 | ||
035 | _a(OCoLC)244638254 | ||
040 |
_aCaPaEBR _cCaPaEBR |
||
050 | 1 | 4 |
_aRM301.25 _b.T49 2006eb |
082 | 0 | 4 |
_a615/.1 _222 |
245 | 0 | 4 |
_aThe textbook of pharmaceutical medicine _h[electronic resource] / _cedited by John P. Griffin and John O'Grady. |
250 | _a5th ed. | ||
260 |
_aOxford ; _aMalden, Mass. : _bBlackwell, _cc2006. |
||
300 |
_ax, 870 p. : _bill. |
||
504 | _aIncludes bibliographical references and index. | ||
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 | _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 | _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. | |
533 |
_aElectronic reproduction. _bPalo Alto, Calif. : _cebrary, _d2013. _nAvailable via World Wide Web. _nAccess may be limited to ebrary affiliated libraries. |
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650 | 0 | _aPharmacology, Experimental. | |
655 | 7 |
_aElectronic books. _2local |
|
700 | 1 |
_aGriffin, J. P. _q(John Parry) |
|
700 | 1 |
_aO'Grady, John, _cProfessor. |
|
710 | 2 | _aebrary, Inc. | |
856 | 4 | 0 |
_uhttp://site.ebrary.com/lib/daystar/Doc?id=10236712 _zAn electronic book accessible through the World Wide Web; click to view |
908 | _a170314 | ||
942 | 0 | 0 | _cEB |
999 |
_c90706 _d90706 |