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Handbook of Process Chromatography, Second Edition: Development, Manufacturing, Validation and Economics
 
 
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Handbook of Process Chromatography, Second Edition: Development, Manufacturing, Validation and Economics [Hardcover]

Lars Hagel (Author), Günter Jagschies (Author), Gail K. Sofer (Author)
5.0 out of 5 stars  See all reviews (1 customer review)

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Book Description

0123740231 978-0123740236 December 22, 2007 2
This book will update the original edition published in 1997. Since the publication of the first edition, the biotechnology and biologics industries have gained extensive knowledge and experience in downstream processing using chromatography and other technologies associated with recovery and purification unit operations. This book will tie that experience together for the next generation of readers.
Updates include:
- sources and productivity
- types of products made today
- experiences in clinical and licensed products
- economics
- current status of validation
- illustrations and tables
- automated column packing
- automated systems
New topics include:
- the use of disposables
- multiproduct versus dedicated production
- design principles for chromatography media and filters
- ultrafiltration principles and optimization
- risk assessments
- characterization studies
- design space
- platform technologies
- process analytical technologies (PATs)
- biogenerics
- comparability assessments

Key Features:
- new approaches to process optimiaztion
- use of patform technologies
- applying risk assessment to process design

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Editorial Reviews

About the Author

Lars Hagel is a Ph.D. in analytical chemistry and also Associate Professor at the University of Uppsala. Dr. Hagel has held different management positions within the R&D department and is now a senior scientific consultant of Pharmacia Biotech. He is a member of the board for The Swedish Centre for Bioseparations, and he chairs the Centre for Bioprocess Technology. Dr. Hagel's research has focused upon practical implications of chromatography theory and he has published a vast number of papers and chapters, with special reference to gel filtration.

Gail Sofer has been consulting with biotechnology and pharmaceutical companies for the past five years through the Fast Trak Validation(r) group of PharmaciaBiotech as the Director of International Validation Development. A series of publications on validation have provided guidance to many in this arena. She is active in organizations such as PDA and ASTM.


Product Details

  • Hardcover: 382 pages
  • Publisher: Academic Press; 2 edition (December 22, 2007)
  • Language: English
  • ISBN-10: 0123740231
  • ISBN-13: 978-0123740236
  • Product Dimensions: 9.7 x 6.6 x 0.8 inches
  • Shipping Weight: 1.7 pounds (View shipping rates and policies)
  • Average Customer Review: 5.0 out of 5 stars  See all reviews (1 customer review)
  • Amazon Best Sellers Rank: #1,709,108 in Books (See Top 100 in Books)

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0 of 1 people found the following review helpful:
5.0 out of 5 stars Excellent reference!, April 23, 2008
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This review is from: Handbook of Process Chromatography, Second Edition: Development, Manufacturing, Validation and Economics (Hardcover)
This book bascially takes you through day 1 of drug manufacturing all the way to the end, when you have deal with regulatory. It also discusses analytical methods which was of great interest to me. Highly recommended for anyone who wants to learn more about this field.
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Inside This Book (learn more)
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
production setups, pressure monitor, matography resin, other adsorptive modes, batch cycling, eluent velocity, zone broadening, chromatography medium, product titers, washout function, biopharma companies, dynamic binding capacity, viral clearance studies, batch frequency, nucleic acid products, ionic capacity, virus filtration, target solute, cleaning validation, membrane adsorbers, multiproduct facilities, buffer costs, chromatographic resin, rapid microbiological methods, eddy dispersion
Key Phrases - Capitalized Phrases (CAPs): (learn more)
New York, Optimization of Chromatographic Separations, International Conference, San Francisco, Separation Technologies, Purification Principles, Validation of Downstream Processes, Oral Presentation, Biopharmaceuticals Today, Process-Design Concepts, Healthcare Bio-Sciences, Academic Press, High Resolution Methods, Trends Biotechnol, Marcel Dekker, Manufacturing of Biopharmaceuticals, Boca Raton, National Meeting, Cost Improvement Options, Fast Flow, Validation Times, Novo Nordisk, Annual Report, American Chemical Society, Experimental Determination of Basic Parameters
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Front Cover | Table of Contents | First Pages | Index | Surprise Me!
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