Editore: Elsevier Science Publishing Co Inc, 2019
ISBN 10: 0128168137 ISBN 13: 9780128168134
Lingua: Inglese
Da: Buchpark, Trebbin, Germania
Condizione: Sehr gut. Zustand: Sehr gut | Sprache: Englisch | Produktart: Bücher.
Da: Majestic Books, Hounslow, Regno Unito
EUR 131,55
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Da: Books Puddle, New York, NY, U.S.A.
EUR 140,55
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Editore: Elsevier Science Publishing Co Inc, 2019
ISBN 10: 0128168137 ISBN 13: 9780128168134
Lingua: Inglese
Da: THE SAINT BOOKSTORE, Southport, Regno Unito
EUR 144,89
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Aggiungi al carrelloPaperback / softback. Condizione: New. New copy - Usually dispatched within 4 working days. 430.
Da: Biblios, Frankfurt am main, HESSE, Germania
EUR 149,35
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Da: GreatBookPrices, Columbia, MD, U.S.A.
EUR 150,98
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Da: Ria Christie Collections, Uxbridge, Regno Unito
EUR 158,96
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Da: GreatBookPricesUK, Woodford Green, Regno Unito
EUR 152,40
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Da: Best Price, Torrance, CA, U.S.A.
EUR 145,42
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Da: GreatBookPrices, Columbia, MD, U.S.A.
EUR 178,65
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Aggiungi al carrelloCondizione: As New. Unread book in perfect condition.
Da: GreatBookPricesUK, Woodford Green, Regno Unito
EUR 180,22
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Da: Brook Bookstore On Demand, Napoli, NA, Italia
EUR 118,06
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Da: Revaluation Books, Exeter, Regno Unito
EUR 132,22
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Aggiungi al carrelloPaperback. Condizione: Brand New. 250 pages. 9.00x6.00x0.63 inches. In Stock. This item is printed on demand.
Editore: Elsevier Science & Technology, Academic Press, 2019
ISBN 10: 0128168137 ISBN 13: 9780128168134
Lingua: Inglese
Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Germania
EUR 131,00
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -The development of a robust drug product requires juggling many competing priorities such as overcoming scientific challenges, following regulatory requirements, and managing business-related concerns. Unfortunately, despite large resources spent on R&D, multifactor productivity of pharmaceuticals is on the decline for several years now. Because of this business reality, pharmaceutical companies have seen a notable change in the traditional operating model and footprint over the past couple of decades. Outsourcing, in particular, has emerged as a successful business model for many pharmaceutical companies looking for ways to strategically increase their R&D capabilities and to augment their in-house resources. How to Integrate Quality by Efficient Design (QbED) in Product Development bridges the gap between theory and practice when it comes to strategic decision-making in a pharmaceutical research scenario. This book will introduce the concept of QbED and focus on various aspects such as patient-centric product designs, platform-based manufacturing technologies, business acuity, and regulatory strategies to balance the challenges in outsourcing with the need for strategic and statistically sound experiments rooted in good science. Detailed discussions will cover pharmaceutical business models, regulatory approval process, quality by design (QbD), business analytics, and manufacturing excellence specifically for small molecules and solid oral dosage forms. With the addition of case studies, flowcharts, diagrams, and data visualizations, How to Integrate Quality by Efficient Design (QbED) in Product Development will be a practical reference to help professionals working in the area of pharmaceutical drug development, strategy, and outsourcing management. Englisch.
Editore: Elsevier Science & Technology|Academic Press, 2019
ISBN 10: 0128168137 ISBN 13: 9780128168134
Lingua: Inglese
Da: moluna, Greven, Germania
EUR 132,74
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Aggiungi al carrelloCondizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. The development of a robust drug product requires juggling many competing priorities such as overcoming scientific challenges, following regulatory requirements, and managing business-related concerns. Unfortunately, despite large resources spent on R&D,.
Editore: Elsevier Science & Technology, Academic Press, 2019
ISBN 10: 0128168137 ISBN 13: 9780128168134
Lingua: Inglese
Da: AHA-BUCH GmbH, Einbeck, Germania
EUR 144,09
Convertire valutaQuantità: 2 disponibili
Aggiungi al carrelloTaschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - The development of a robust drug product requires juggling many competing priorities such as overcoming scientific challenges, following regulatory requirements, and managing business-related concerns. Unfortunately, despite large resources spent on R&D, multifactor productivity of pharmaceuticals is on the decline for several years now. Because of this business reality, pharmaceutical companies have seen a notable change in the traditional operating model and footprint over the past couple of decades. Outsourcing, in particular, has emerged as a successful business model for many pharmaceutical companies looking for ways to strategically increase their R&D capabilities and to augment their in-house resources. How to Integrate Quality by Efficient Design (QbED) in Product Development bridges the gap between theory and practice when it comes to strategic decision-making in a pharmaceutical research scenario. This book will introduce the concept of QbED and focus on various aspects such as patient-centric product designs, platform-based manufacturing technologies, business acuity, and regulatory strategies to balance the challenges in outsourcing with the need for strategic and statistically sound experiments rooted in good science. Detailed discussions will cover pharmaceutical business models, regulatory approval process, quality by design (QbD), business analytics, and manufacturing excellence specifically for small molecules and solid oral dosage forms. With the addition of case studies, flowcharts, diagrams, and data visualizations, How to Integrate Quality by Efficient Design (QbED) in Product Development will be a practical reference to help professionals working in the area of pharmaceutical drug development, strategy, and outsourcing management.