Dose Finding in Drug Development

Please use this identifier to cite or link to this item: 192.168.6.56/handle/123456789/47568

Full metadata record

DC Field	Value	Language
dc.contributor.editor	Ting, Naitee	-
dc.contributor.editor	W. Wong	-
dc.contributor.editor	M. Gail	-
dc.contributor.editor	A. Tsiatis	-
dc.contributor.editor	J. Samet	-
dc.date.accessioned	2019-02-26T05:49:56Z	-
dc.date.available	2019-02-26T05:49:56Z	-
dc.date.issued	2006	-
dc.identifier.isbn	978-0387-29074-4	-
dc.identifier.isbn	0-387-29074-5	en_US
dc.identifier.uri	http://10.6.20.12:80/handle/123456789/47568	-
dc.description	This book introduces the drug development process, the design and analysis of clinical trials. Many of the discussions are based on applications of statistical methods in the design and analysis of dose response studies. Although the book is prepared mainly for statisticians/biostatisticians, it also serves as a useful reference to a variety of professionals working for the pharmaceutical industry. The potential readers include pharmacokienticists, clinical scientists, clinical pharmacologists, pharmacists, project managers, pharmaceutical scientists, clinicians, programmers, data managers, regulatory specialists, and study report writers.	-
dc.language.iso	en	en_US
dc.publisher	Springer Science Business Media, LLC	en_US
dc.subject	Doses	en_US
dc.title	Dose Finding in Drug Development	en_US
dc.type	Book	en_US
Appears in Collections:	Medical Labratory

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Naitee Ting.pdf		4.67 MB	Adobe PDF	View/Open