Sprache: Englisch
Verlag: Stewart, Tabori & Chang Inc, 1989
ISBN 10: 155670061X ISBN 13: 9781556700613
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Hardcover. Zustand: Fine. Zustand des Schutzumschlags: Near Fine. Price tag on front cover.
Hardcover. Zustand: Fine. Zustand des Schutzumschlags: Fine. 1st Edition. hardback book and dust jacket in fine condition,inscribed by the author,then signed [love,andy,5/24/89]. Inscribed by Author(s).
Sprache: Englisch
Verlag: Stewart. Tabori & Chang, New York, 1989
ISBN 10: 155670061X ISBN 13: 9781556700613
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In den Warenkorb160x110mm. Zustand: Very Good. First. 111pp Fully illustrated in colour & b&w archive photographs. There is a small stain on the fep.
Verlag: STEWART, TABORI & CHANG, NEW YORK, 1989
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MAROON CLOTH. Zustand: FINE. Zustand des Schutzumschlags: FINE. FIRST EDITION, FIRST PRINTING. DUST JACKET IS IN A PROTECTIVE PLASTIC COVER. Size: SQUARE QUARTO.
Sprache: Englisch
Verlag: Stewart, Tabori & Chang,, New York,, 1989
ISBN 10: 155670061X ISBN 13: 9781556700613
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In den WarenkorbHardback. Zustand: Fine. First Edition. Hardback. Dust Jacket. 4to. pp 111. 26cm by 26cm. Original publisher's burgundy cloth, lettered gilt at the spine. Copiously illustrated in colour and black and white throughout. ISBN: 155670061X Fine in fine dust jacket.
hardcover. Zustand: New. In shrink wrap. Looks like an interesting title!
hardcover. Zustand: Sehr gut. Seiten; 9780470552346.2 Gewicht in Gramm: 1.
Wiley-Verlag, Hardcover, sehr guter Zustand, h4.
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In den WarenkorbZustand: New. pp. 208.
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In den WarenkorbPaperback. Zustand: Brand New. 208 pages. 9.00x6.00x0.71 inches. In Stock.
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Sprache: Englisch
Verlag: Elsevier Science Publishing Co Inc, 2019
ISBN 10: 0128094125 ISBN 13: 9780128094129
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In den WarenkorbPaperback / softback. Zustand: New. New copy - Usually dispatched within 4 working days.
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Zustand: New. pp. 208.
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In den WarenkorbZustand: New.
Hardcover. Zustand: new. New Copy. Customer Service Guaranteed.
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Taschenbuch. Zustand: Neu. Principles of Parenteral Solution Validation | A Practical Lifecycle Approach | Igor Gorsky (u. a.) | Taschenbuch | Englisch | 2019 | Elsevier Science | EAN 9780128094129 | Verantwortliche Person für die EU: Libri GmbH, Europaallee 1, 36244 Bad Hersfeld, gpsr[at]libri[dot]de | Anbieter: preigu.
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In den WarenkorbZustand: New. A. HAMID MOLLAH, PhD, is the Head of Quality Engineering and Validation at XOMA. He has also held positions at Genentech and Baxter. He is a RAPS Certified Regulatory Affairs Professional and ASQ Certified Quality Engineer.Dr. MIKE LONG, has two decades of .
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In den WarenkorbHardcover. Zustand: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.
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In den WarenkorbZustand: As New. Unread book in perfect condition.
Buch. Zustand: Neu. Neuware - This book contains both the theory and practice of risk management (RM) and provides the background, tools, and application of risk in pharmaceutical and biologics manufacturing and operations. It includes case studies and specific examples of use of RM for biological and pharmaceutical product manufacture. The book also includes useful references and a bibliography for the reader who wishes to gain additional knowledge in the subject. It aids in assisting both industry and regulatory agencies to implement compliant and effective risk management approaches, and includes case studies to help with understanding.
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In den WarenkorbZustand: new. Questo è un articolo print on demand.
Sprache: Englisch
Verlag: Elsevier Science Nov 2019, 2019
ISBN 10: 0128094125 ISBN 13: 9780128094129
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 -Principles of Parenteral Solution Validation: A Practical Lifecycle Approach covers all aspects involved in the development and process validation of a parenteral product. By using a lifecycle approach, this book discusses the latest technology, compliance developments, and regulatory considerations and trends, from process design, to divesting. As part of the Expertise in Pharmaceutical Process Technology series edited by Michael Levin, this book incorporates numerous case studies and real-world examples that address timely problems and offer solutions to the daily challenges facing practitioners in this area. 298 pp. Englisch.
Sprache: Englisch
Verlag: John Wiley & Sons Inc, New York, 2013
ISBN 10: 0470552344 ISBN 13: 9780470552346
Anbieter: Grand Eagle Retail, Bensenville, IL, USA
Erstausgabe Print-on-Demand
Hardcover. Zustand: new. Hardcover. Sets forth tested and proven risk management practices in drug manufacturing Risk management is essential for safe and efficient pharmaceutical and biopharmaceutical manufacturing, control, and distribution. With this book as their guide, readers involved in all facets of drug manufacturing have a single, expertly written, and organized resource to guide them through all facets of risk management and analysis. It sets forth a solid foundation in risk management concepts and then explains how these concepts are applied to drug manufacturing. Risk Management Applications in Pharmaceutical and Biopharmaceutical Manufacturing features contributions from leading international experts in risk management and drug manufacturing. These contributions reflect the latest research, practices, and industry standards as well as the authors' firsthand experience. Readers can turn to the book for: Basic foundation of risk management principles, practices, and applicationsTested and proven tools and methods for managing risk in pharmaceutical and biopharmaceutical product manufacturing processesRecent FDA guidelines, EU regulations, and international standards governing the application of risk management to drug manufacturingCase studies and detailed examples demonstrating the use and results of applying risk management principles to drug product manufacturingBibliography and extensive references leading to the literature and helpful resources in the field With its unique focus on the application of risk management to biopharmaceutical and pharmaceutical manufacturing, this book is an essential resource for pharmaceutical and process engineers as well as safety and compliance professionals involved in drug manufacturing. This book contains both the theory and practice of risk management (RM) and provides the background, tools, and application of risk in pharmaceutical and biologics manufacturing and operations. It includes case studies and specific examples of use of RM for biological and pharmaceutical product manufacture. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.
Taschenbuch. Zustand: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Principles of Parenteral Solution Validation: A Practical Lifecycle Approach covers all aspects involved in the development and process validation of a parenteral product. By using a lifecycle approach, this book discusses the latest technology, compliance developments, and regulatory considerations and trends, from process design, to divesting. As part of the Expertise in Pharmaceutical Process Technology series edited by Michael Levin, this book incorporates numerous case studies and real-world examples that address timely problems and offer solutions to the daily challenges facing practitioners in this area.
Sprache: Englisch
Verlag: John Wiley & Sons Inc, New York, 2013
ISBN 10: 0470552344 ISBN 13: 9780470552346
Anbieter: CitiRetail, Stevenage, Vereinigtes Königreich
Erstausgabe Print-on-Demand
EUR 161,66
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In den WarenkorbHardcover. Zustand: new. Hardcover. Sets forth tested and proven risk management practices in drug manufacturing Risk management is essential for safe and efficient pharmaceutical and biopharmaceutical manufacturing, control, and distribution. With this book as their guide, readers involved in all facets of drug manufacturing have a single, expertly written, and organized resource to guide them through all facets of risk management and analysis. It sets forth a solid foundation in risk management concepts and then explains how these concepts are applied to drug manufacturing. Risk Management Applications in Pharmaceutical and Biopharmaceutical Manufacturing features contributions from leading international experts in risk management and drug manufacturing. These contributions reflect the latest research, practices, and industry standards as well as the authors' firsthand experience. Readers can turn to the book for: Basic foundation of risk management principles, practices, and applicationsTested and proven tools and methods for managing risk in pharmaceutical and biopharmaceutical product manufacturing processesRecent FDA guidelines, EU regulations, and international standards governing the application of risk management to drug manufacturingCase studies and detailed examples demonstrating the use and results of applying risk management principles to drug product manufacturingBibliography and extensive references leading to the literature and helpful resources in the field With its unique focus on the application of risk management to biopharmaceutical and pharmaceutical manufacturing, this book is an essential resource for pharmaceutical and process engineers as well as safety and compliance professionals involved in drug manufacturing. This book contains both the theory and practice of risk management (RM) and provides the background, tools, and application of risk in pharmaceutical and biologics manufacturing and operations. It includes case studies and specific examples of use of RM for biological and pharmaceutical product manufacture. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.