Sprache: Englisch
Verlag: Springer (India) Private Limited, 2009
ISBN 10: 8184891512 ISBN 13: 9788184891515
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Verlag: Springer, 2006
ISBN 10: 0387290745 ISBN 13: 9780387290744
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In den WarenkorbHardback. Zustand: Very Good. No Jacket. First edition. 1st 2006. Very good condition with no wrapper. Statistics for Biology and Health series. This book introduces the drug development process in clinical trials, including its design and analysis. Yellow and purple matt boards. Boards scuffed, marked, and faded to spine. Corners rubbed. A few corner creases to contents. One or two highlights to margins. Packaged with care and promptly dispatched!
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Taschenbuch. Zustand: Neu. Dose Finding in Drug Development | Naitee Ting | Taschenbuch | Statistics for Biology and Health | xiv | Englisch | 2010 | Springer | EAN 9781441921154 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.
Sprache: Englisch
Verlag: Springer New York, Springer US Nov 2010, 2010
ISBN 10: 144192115X ISBN 13: 9781441921154
Anbieter: buchversandmimpf2000, Emtmannsberg, BAYE, Deutschland
Taschenbuch. Zustand: Neu. Neuware -This book emphasizes dose selection issues from a statistical point of view. It presentsstatisticalapplicationsinthedesignandanalysisofdose¿responsestudies. The importance of this subject can be found from the International Conference on Harmonization (ICH) E4 Guidance document. Establishing the dose¿response relationship is one of the most important act- ities in developing a new drug. A clinical development program for a new drug can be broadly divided into four phases ¿ namely Phases I, II, III, and IV. Phase I clinical trials are designed to study the clinical pharmacology. Information - tained from these studies will help in designing Phase II studies. Dose¿response relationshipsareusuallystudiedinPhaseII.PhaseIIIclinicaltrialsarelarge-scale, long-term studies. These studies serve to con rm ndings from Phases I and II. ResultsobtainedfromPhasesI,II,andIIIclinicaltrialswouldthenbedocumented and submitted to regulatory agencies for drug approval. In the United States, - viewers from Food and Drug Administration (FDA) review these documents and make a decision to approve or to reject this New Drug Application (NDA). If the new drug is approved, then Phase IV studies can be started. Phase IV clinical trials are also known as postmarketing studies.Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg 264 pp. Englisch.
Sprache: Englisch
Verlag: Springer New York, Springer US, 2010
ISBN 10: 144192115X ISBN 13: 9781441921154
Anbieter: AHA-BUCH GmbH, Einbeck, Deutschland
Taschenbuch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - This book emphasizes dose selection issues from a statistical point of view. It presentsstatisticalapplicationsinthedesignandanalysisofdose-responsestudies. The importance of this subject can be found from the International Conference on Harmonization (ICH) E4 Guidance document. Establishing the dose-response relationship is one of the most important act- ities in developing a new drug. A clinical development program for a new drug can be broadly divided into four phases - namely Phases I, II, III, and IV. Phase I clinical trials are designed to study the clinical pharmacology. Information - tained from these studies will help in designing Phase II studies. Dose-response relationshipsareusuallystudiedinPhaseII.PhaseIIIclinicaltrialsarelarge-scale, long-term studies. These studies serve to con rm ndings from Phases I and II. ResultsobtainedfromPhasesI,II,andIIIclinicaltrialswouldthenbedocumented and submitted to regulatory agencies for drug approval. In the United States, - viewers from Food and Drug Administration (FDA) review these documents and make a decision to approve or to reject this New Drug Application (NDA). If the new drug is approved, then Phase IV studies can be started. Phase IV clinical trials are also known as postmarketing studies.
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In den WarenkorbPaperback. Zustand: Brand New. 248 pages. 8.90x5.98x0.87 inches. In Stock.
Sprache: Englisch
Verlag: Springer, 2006
Anbieter: Books in my Basket, New Delhi, Indien
Hardcover. Zustand: New. ISBN:9780387290744.
Anbieter: moluna, Greven, Deutschland
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In den WarenkorbGebunden. Zustand: New. Introduces the drug development process, the design and analysis of clinical trialsPresents statistical applications in the design and analysis of dose response studiesExamines important procedural steps from a pharmaceutical industry persp.
Anbieter: Mispah books, Redhill, SURRE, Vereinigtes Königreich
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In den WarenkorbHardcover. Zustand: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.
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In den WarenkorbPaperback. Zustand: Like New. Like New. book.
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In den WarenkorbZustand: new. Questo è un articolo print on demand.
Sprache: Englisch
Verlag: Springer-Verlag New York Inc., 2010
ISBN 10: 144192115X ISBN 13: 9781441921154
Anbieter: THE SAINT BOOKSTORE, Southport, Vereinigtes Königreich
EUR 165,50
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In den WarenkorbPaperback / softback. Zustand: New. This item is printed on demand. New copy - Usually dispatched within 5-9 working days.
Anbieter: moluna, Greven, Deutschland
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In den WarenkorbZustand: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Introduces the drug development process, the design and analysis of clinical trialsPresents statistical applications in the design and analysis of dose response studiesExamines important procedural steps from a pharmaceutical industry persp.
Sprache: Englisch
Verlag: Springer New York Nov 2010, 2010
ISBN 10: 144192115X ISBN 13: 9781441921154
Anbieter: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Deutschland
Taschenbuch. Zustand: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -If you have ever wondered when visiting the pharmacy how the dosage of your prescription is determined this book will answer your questions. Dosing information on drug labels is based on discussion between the pharmaceutical manufacturer and the drug regulatory agency, and the label is a summary of results obtained from many scientific experiments. The book introduces the drug development process, the design and the analysis of clinical trials. Many of the discussions are based on applications of statistical methods in the design and analysis of dose response studies. Important procedural steps from a pharmaceutical industry perspective are also examined. 264 pp. Englisch.