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Combination Drug Products - Siegel
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Siegel:

Combination Drug Products - novo libro

2013, ISBN: 9780470050941

[ED: Buch], [PU: John Wiley & Sons], Neuware - A step-by-step, integrated approach for successful, FDA-approved combination drug products Using a proven integrated approach to combination… mais…

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Development and Approval of Combination Products - Siegel, Evan B.
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Siegel, Evan B.:

Development and Approval of Combination Products - novo libro

ISBN: 9780470050941

A step-by-step, integrated approach for successful, FDA-approved combination drug products Using a proven integrated approach to combination drug development, this book guides you step… mais…

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Development and Approval of Combination Products - Evan B. Siegel
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Evan B. Siegel:
Development and Approval of Combination Products - encadernado, livro de bolso

ISBN: 9780470050941

Hardback, [PU: John Wiley & Sons Inc], A step-by-step, integrated approach for successful, FDA-approved combination drug products Using a proven integrated approach to combination drug d… mais…

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Combination Drug Products - Siegel
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Siegel:
Combination Drug Products - encadernado, livro de bolso

2008, ISBN: 0470050942

Gebundene Ausgabe HEALTH & FITNESS / Safety, mit Schutzumschlag neu, [PU:John Wiley & Sons]

Custos de envio:Versandkostenfrei innerhalb der BRD. (EUR 0.00) MARZIES.de Buch- und Medienhandel, 14621 Schönwalde-Glien
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Development and Approval of Combination Products - Evan B. Siegel
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Evan B. Siegel:
Development and Approval of Combination Products - encadernado, livro de bolso

2008, ISBN: 9780470050941

Hardcover, Buch, [PU: Wiley-Blackwell]

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Development and Approval of Combination Products: A Regulatory Perspective

A step-by-step, integrated approach for successful, FDA-approved combination drug products Using a proven integrated approach to combination drug development, this book guides you step by step through all the preclinical, clinical, and manufacturing stages. Written from an FDA regulatory perspective, the book not only enables you to bring a successful combination drug product to market, it also sets forth the most efficient and effective path to FDA approval. The book begins with an introductory chapter presenting definitions and basic regulatory principles of combination products. Next, it reviews manufacturing and controls, preclinical testing models, pharmacology, clinical testing, regulatory submissions, FDA reviews, and approvals. Among the key topics examined are: * The pharmacology, safety pharmacology, and toxicology supporting human clinical trials of combination products * Approaches to clinical trial protocol design and execution * Chemical, physicochemical, and analytical aspects of manufacturing controls and validation that lead to stable components for combination products * Key sponsor/FDA meetings and negotiations essential for approval and commercialization Case studies involving such actual combination products as Mylotarg, Herceptin, and HercepTest help you better understand how to implement the author's practical guidelines. References at the end of each chapter enable you to find more information on any stage of the development, manufacturing and approval processes. This book is ideal for researchers, regulators, academics, project managers, and executives involved in the complex process of combination product development. Not only does itoffer a comprehensive guide to the technical aspects of the field, it also integrates all ofthese technical aspects into a unified, effective approach to help ensure a successful, approved product.

Dados detalhados do livro - Development and Approval of Combination Products: A Regulatory Perspective


EAN (ISBN-13): 9780470050941
ISBN (ISBN-10): 0470050942
Livro de capa dura
Ano de publicação: 2008
Editor/Editora: John Wiley & Sons
215 Páginas
Peso: 0,517 kg
Língua: eng/Englisch

Livro na base de dados desde 2008-06-04T00:00:03+01:00 (Lisbon)
Página de detalhes modificada pela última vez em 2021-10-24T17:06:41+01:00 (Lisbon)
Número ISBN/EAN: 9780470050941

Número ISBN - Ortografia alternativa:
0-470-05094-2, 978-0-470-05094-1
Ortografia alternativa e termos de pesquisa relacionados:
Autor do livro: siegel evan, john wiley sons
Título do livro: products


Dados da editora

Autor: Evan B. Siegel
Título: Development and Approval of Combination Products - A Regulatory Perspective
Editora: John Wiley & Sons
216 Páginas
Ano de publicação: 2008-06-05
Peso: 0,517 kg
Língua: Inglês
115,00 € (DE)
No longer receiving updates
161mm x 240mm x 19mm

BB; Hardcover, Softcover / Chemie; Medizinische Chemie, Pharmazeutische Chemie; Apparatetechnik u. Biosensoren; Arzneimittelentwicklung; Bioinstrumentation & Biosensors; Biomedical Engineering; Biomedizintechnik; Chemie; Chemistry; Drug Discovery & Development; Medical Science; Medizin; Pharmacology & Pharmaceutical Medicine; Pharmakologie u. Pharmazeutische Medizin; Wirkstoffforschung u. -entwicklung; Apparatetechnik u. Biosensoren; Wirkstoffforschung u. -entwicklung; Pharmakologie u. Pharmazeutische Medizin

A step-by-step, integrated approach for successful, FDA-approved combination drug products Using a proven integrated approach to combination drug development, this book guides you step by step through all the preclinical, clinical, and manufacturing stages. Written from an FDA regulatory perspective, the book not only enables you to bring a successful combination drug product to market, it also sets forth the most efficient and effective path to FDA approval. The book begins with an introductory chapter presenting definitions and basic regulatory principles of combination products. Next, it reviews manufacturing and controls, preclinical testing models, pharmacology, clinical testing, regulatory submissions, FDA reviews, and approvals. Among the key topics examined are: * The pharmacology, safety pharmacology, and toxicology supporting human clinical trials of combination products * Approaches to clinical trial protocol design and execution * Chemical, physicochemical, and analytical aspects of manufacturing controls and validation that lead to stable components for combination products * Key sponsor/FDA meetings and negotiations essential for approval and commercialization Case studies involving such actual combination products as Mylotarg, Herceptin, and HercepTest help you better understand how to implement the author's practical guidelines. References at the end of each chapter enable you to find more information on any stage of the development, manufacturing and approval processes. This book is ideal for researchers, regulators, academics, project managers, and executives involved in the complex process of combination product development. Not only does itoffer a comprehensive guide to the technical aspects of the field, it also integrates all ofthese technical aspects into a unified, effective approach to help ensure a successful, approved product.

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