Filtration and Purification in the Biopharmaceutical Industry, Third Edition

Author:   Maik W. Jornitz
Publisher:   Taylor & Francis Ltd
Edition:   3rd edition
ISBN:  

9781138056749


Pages:   672
Publication Date:   12 July 2019
Format:   Hardback
Availability:   In Print   Availability explained
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Filtration and Purification in the Biopharmaceutical Industry, Third Edition


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Full Product Details

Author:   Maik W. Jornitz
Publisher:   Taylor & Francis Ltd
Imprint:   CRC Press
Edition:   3rd edition
Weight:   1.370kg
ISBN:  

9781138056749


ISBN 10:   113805674
Pages:   672
Publication Date:   12 July 2019
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Active
Availability:   In Print   Availability explained
This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us.

Table of Contents

Depth and Lenticular Filtration Prefiltration Charge-Modified Filter Media Filter Designs Quality Assurance of Filter Manufacture Pore Size and Distributions Extractables and Compatibilities of Filters Bacterial Biofilms Filtrative Particle Removal Integrity Testing Sizing of Membrane Filter Systems Filter Housings Cross-Flow Filtration Protein Adsorption on Membrane Filters Microbial Retention Testing Filtration of Viral Contamination Membrane Chromatography LAL Testing Air Filtration in the Biopharmaceutical Industry Sterility Testing with Membrane Filters Cell Harvesting Downstream Processing Important Factors in Media and Buffer Filtration The Filtration of Blood and Blood Fractions The Operation of the FDA The Operation of the EMEA Validation of Particle Counters Validation of Filtrative Sterilization

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Author Information

Maik W. Jornitz, President and CEO of G-CON Manufacturing Inc. and founder of Bioprocess Resources LLC, is a technical expert with over 30 years of experience in bioprocesses, especially sterilizing grade filtration and single-use technologies, including regulatory requirements, integrity testing, systems design, and optimization. Jornitz has published 10 books, 15 book chapters and over 100 scientific papers. He is Chair of the PDA Science Advisory Board, member of multiple PDA Task Forces. He is working member of BPOG, ASTM, an advisory board member of the Biotechnology Industry Council, ICAV and multiple science journals. He recently has been recognized as one of the top ten global industry influencers. As a faculty member of various training activities, including PDA TRI, he trains members of the industry and regulatory authorities on a frequent basis. He received his M.Eng. in Bioengineering at the University of Applied Sciences in Hamburg, Germany and accomplished the PED program at IMD Business School in Lausanne, Switzerland

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