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Ajouter au panierHardcover. Etat : Very Good. 4th Edition. Fourth edition. Shipping weight over 1kg. Clean and bright interior with unmarked text, free of inscriptions and stamps, firmly bound. Gentle wear to the lower outer page corners. Boards show small corner creases; two short edge-tears to the upper spine (appear glued). Issued without a dust jacket.
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Edité par TAYLOR & FRANCIS NP EXCLUSIVE(CBS), 2024
ISBN 10 : 0367697629 ISBN 13 : 9780367697624
Langue: anglais
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Ajouter au panierEtat : New. Brand New! Fast Delivery This is an International Edition and ship within 24-48 hours. Deliver by FedEx and Dhl, & Aramex, UPS, & USPS and we do accept APO and PO BOX Addresses. Order can be delivered worldwide within 7-10 days and we do have flat rate for up to 2LB. Extra shipping charges will be requested if the Book weight is more than 5 LB. This Item May be shipped from India, United states & United Kingdom. Depending on your location and availability.
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Ajouter au panierHardcover. Etat : Like New. Like New. book.
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Ajouter au panierHardcover. Etat : Brand New. 4th edition. 552 pages. 10.00x7.00x0.98 inches. In Stock.
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Ajouter au panierBuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -The fourth edition of Process Validation in Manufacturing of Biopharmaceuticals is a practical and comprehensive resource illustrating the different approaches for successful validation of biopharmaceutical processes. A pivotal text in its field, this new edition provides guidelines and current practices, contains industrial case studies, and is expanded to include in-depth analysis of the new Process Validation (PV) guidance from the US FDA.Key Features:Offers readers a thorough understanding of the key concepts that form the basis of a good process validation program for biopharmaceuticals.Includes case studies from the various industry leaders that demonstrate application of these concepts.Discusses the use of modern tools such as multivariate analysis for facilitating a process validation exercise.Covers process characterization techniques for scaling down unit operations in biopharmaceutical manufacturing, including chromatography, chemical modification reactions, ultrafiltration, and microfiltration, and practical methods to test raw materials and in-process samples.Providing a thorough understanding of the key concepts that form the basis of a good process validation program, this book will help readers ensure that PV is carried out and exceeds expectations. Fully illustrated, this is a much-needed practical guide for biopharmaceutical manufacturers. 414 pp. Englisch.
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EUR 195,37
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Ajouter au panierEtat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. ANURAG S. RATHORE is an Institute Chair Professor at the Department of Chemical Engineering, Indian Institute of Technology, Delhi, India. He is also the Coordinator for the DBT COE for Biopharmaceutical Technology. His areas of interest include process .
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Ajouter au panierHRD. Etat : New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.
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Ajouter au panierHRD. Etat : New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.
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Ajouter au panierBuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - The fourth edition of Process Validation in Manufacturing of Biopharmaceuticals is a practical and comprehensive resource illustrating the different approaches for successful validation of biopharmaceutical processes. A pivotal text in its field, this new edition provides guidelines and current practices, contains industrial case studies, and is expanded to include in-depth analysis of the new Process Validation (PV) guidance from the US FDA.Key Features:Offers readers a thorough understanding of the key concepts that form the basis of a good process validation program for biopharmaceuticals.Includes case studies from the various industry leaders that demonstrate application of these concepts.Discusses the use of modern tools such as multivariate analysis for facilitating a process validation exercise.Covers process characterization techniques for scaling down unit operations in biopharmaceutical manufacturing, including chromatography, chemical modification reactions, ultrafiltration, and microfiltration, and practical methods to test raw materials and in-process samples.Providing a thorough understanding of the key concepts that form the basis of a good process validation program, this book will help readers ensure that PV is carried out and exceeds expectations. Fully illustrated, this is a much-needed practical guide for biopharmaceutical manufacturers.
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Ajouter au panierBuch. Etat : Neu. Process Validation in Manufacturing of Biopharmaceuticals | Anurag Singh Rathore (u. a.) | Buch | Einband - fest (Hardcover) | Englisch | 2023 | CRC Press | EAN 9780367697624 | Verantwortliche Person für die EU: Libri GmbH, Europaallee 1, 36244 Bad Hersfeld, gpsr[at]libri[dot]de | Anbieter: preigu Print on Demand.