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Emily P. Wen - Vaccine Development and Manufacturing - 9780470261941 - V9780470261941
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Vaccine Development and Manufacturing

€ 199.22
FREE Delivery in Ireland
Description for Vaccine Development and Manufacturing Hardback. Vaccine Production and Manufacturing is a valuable reference on how to produce a vaccine, from beginning to end. It addresses all classes of vaccines from a processing, production, and regulatory viewpoint. It covers everything from fermentation, purification, and formulation to regulatory filing and facility design. Editor(s): Wen, Emily P.; Ellis, Ronald J.; Pujar, Narahari S. Series: Wiley Series in Biotechnology and Bioengineering. Num Pages: 456 pages. BIC Classification: MMG; TDCW. Category: (P) Professional & Vocational. Dimension: 243 x 158 x 28. Weight in Grams: 756.

Vaccine Manufacturing and Production is an invaluable reference on how to produce a vaccine - from beginning to end - addressing all classes of vaccines from a processing, production, and regulatory viewpoint. It will provide comprehensive information on the various fields involved in the production of vaccines, from fermentation, purification, formulation, to regulatory filing and facility designs. In recent years, there have been tremendous advances in all aspects of vaccine manufacturing. Improved technology and growth media have been developed for the production of cell culture with high cell density or fermentation. Vaccine Manufacturing and Production will serve as a reference on all aspects of vaccine production by providing an in-depth description of the available technologies for making different types of vaccines and the current thinking in facility designs and supply issues. This book will provide insight to the issues scientists face when producing a vaccine, the steps that are involved, and will serve as a reference tool regarding state-of-the-art vaccine manufacturing technologies and facility set-up.

Highlights include:

  • Comprehensive coverage of vaccine production : from a process point of view- fermentation to purification to formulation developments; from a production point of view - from facility design to manufacturing; and from a regulatory point of view - requirements from government agencies
  • Authors from different major pharmaceutical and biotechnology companies
  • Describes the challenges and issues involved in vaccine production and manufacturing of the different classes of vaccines, an area not covered by other books currently on the market

Product Details

Format
Hardback
Publication date
2015
Publisher
John Wiley and Sons Ltd United States
Number of pages
456
Condition
New
Series
Wiley Series in Biotechnology and Bioengineering
Number of Pages
464
Place of Publication
New York, United States
ISBN
9780470261941
SKU
V9780470261941
Shipping Time
Usually ships in 7 to 11 working days
Ref
99-50

About Emily P. Wen
EMILY P. WEN, PhD, is currently a Research Fellow at the Merck Research Laboratory in the department of Vaccine Process Development. Dr. Wen has led process developments for several major vaccine products from Phase I to Phase III clinical trials, including vaccines against hepatitis B, Haemophilus influenzae type b, Pneumococcal, Meningococcal, and Group B Streptococcus. RONALD ELLIS, PhD, is Chief Technology Officer at FutuRx Ltd in Israel. Dr. Ellis has more than 30 years of industry experience in line and senior management in many companies, including roles as project leader and champion of projects that resulted in five licensed vaccines which accrue ~$4B in annual sales. He is the founding and incumbent Editor-in-Chief of the MedLine-/PubMed-indexed journal Human Vaccines & Immunotherapeutics. NARAHARI S. PUJAR, PhD, MBA, is currently an Executive Director and Integrated Product Leader in the Vaccine Business Line at Merck & Co., Inc. Dr. Pujar has contributed to a variety of vaccines and biologics products and product candidates. He is an active member of the American Chemical Society and was the past chair of the Division of Biochemical Technology.

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