Published by Academic Press 2015-01-08, 2015
ISBN 10: 0124202462 ISBN 13: 9780124202467
Language: English
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Add to basketHardcover. Condition: Brand New. 1st edition. 360 pages. 9.00x6.00x1.00 inches. In Stock.
Published by Elsevier Science Publishing Co Inc, 2015
ISBN 10: 0124202462 ISBN 13: 9780124202467
Language: English
Seller: THE SAINT BOOKSTORE, Southport, United Kingdom
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Add to basketHardback. Condition: New. New copy - Usually dispatched within 4 working days. 711.
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Seller: Antiquariat Buchhandel Daniel Viertel, Diez, Germany
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Add to basketGr.-8° Gebundene Ausgabe, Condition: Sehr gut. 1. 360 S. in gutem Zustand 29834 ISBN 9780124202467 Sprache: Englisch Gewicht in Gramm: 750.
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Add to basketCondition: new. Questo è un articolo print on demand.
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Add to basketBuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -The pharmaceutical industry is currently operating under a business model that is not sustainable for the future. Given the high costs associated with drug development, there is a vital need to reform this process in order to provide safe and effective drugs while still securing a profit. Re-Engineering Clinical Trials evaluates the trends and challenges associated with the current drug development process and presents solutions that integrate the use of modern communication technologies, innovations and novel enrichment designs. This book focuses on the need to simplify drug development and offers you well-established methodologies and best practices based on real-world experiences from expert authors across industry and academia. Written for all those involved in clinical research, development and clinical trial design, this book provides a unique and valuable resource for streamlining the process, containing costs and increasing drug safety and effectiveness. Englisch.
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Add to basketBuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - The pharmaceutical industry is currently operating under a business model that is not sustainable for the future. Given the high costs associated with drug development, there is a vital need to reform this process in order to provide safe and effective drugs while still securing a profit. Re-Engineering Clinical Trials evaluates the trends and challenges associated with the current drug development process and presents solutions that integrate the use of modern communication technologies, innovations and novel enrichment designs. This book focuses on the need to simplify drug development and offers you well-established methodologies and best practices based on real-world experiences from expert authors across industry and academia. Written for all those involved in clinical research, development and clinical trial design, this book provides a unique and valuable resource for streamlining the process, containing costs and increasing drug safety and effectiveness.