バイオ薬剤の製造におけるプロセス認証(第4版)<br>Process Validation in Manufacturing of Biopharmaceuticals (Biotechnology and Bioprocessing) (4TH)

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バイオ薬剤の製造におけるプロセス認証(第4版)
Process Validation in Manufacturing of Biopharmaceuticals (Biotechnology and Bioprocessing) (4TH)

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  • 製本 Hardcover:ハードカバー版/ページ数 392 p.
  • 言語 ENG
  • 商品コード 9780367697624
  • DDC分類 615.19

Full Description

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.

Contents

The Evolution of Modern Process Validation: Commentary on the U.S. Food and Drug Administration's 2011 Guidance for Industry, Process Validation Principles and Practices
Hal Baseman




Applications of Failure Modes and Effects Analysis to Biotechnology Manufacturing Processes
Robert J. Seely and John Haury




Process Characterization
James E. Seely




Scale-Down Models for Microbial and Mammalian Cell Culture Processes: Approaches and Applications
Ravali Raju et al.




Scale-Down Models for Purification Processes: Approaches and Application
Arch Creasy et al.




Principles of Quality Risk Management for Validation
Tiffany Baker and Patrick Mains




Lifespan Studies for Chromatography and Filtration Media
Anurag S. Rathore and Gail Sofer




Analytical Test Methods for Well-Characterized Biological and Biotechnological Products
Nadine Ritter and John McEntire




Adventitious Agents: Concerns and Testing for Biopharmaceuticals
Raymond W. Nims et al.




Biotech Facility Design for Validation
Phil DeSantis




Process Validation at Contract Manufacturing Organizations: Approaches, Incentives, Benefits, and Risks
Maria Wik and Scott Rudge




Validation of a Filtration Step
Jennifer Campbell et al.




Validation of Continuous Bioprocesses
Marc Bisschops and Mark Schofield




Role of Multivariate Analysis in Process Validation
Anurag S. Rathore and Vishwanath Hebbi




Process Development for Plasmid DNA Production
Frank Agbogdo et al.

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