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Downstream Industrial Biotechnology : Recovery and Purification /
"Universities worldwide are establishing biomanufacturing centers, and demand is growing for a workforce trained in this discipline. Downstream Recovery and Purification is an affordable, accessible desk reference on biomanufacturing for professionals, instructors, and students. With informatio...
| Clasificación: | Libro Electrónico |
|---|---|
| Otros Autores: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Hoboken, New Jersey :
Wiley,
[2013]
|
| Temas: | |
| Acceso en línea: | Texto completo |
MARC
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| 130 | 0 | |a Encyclopedia of industrial biotechnology. |k Selections. | |
| 245 | 1 | 0 | |a Downstream Industrial Biotechnology : |b Recovery and Purification / |c edited by Michael C. Flickinger. |
| 260 | |a Hoboken, New Jersey : |b Wiley, |c [2013] | ||
| 300 | |a 1 online resource (xiv, 858 pages) : |b illustrations | ||
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| 520 | |a "Universities worldwide are establishing biomanufacturing centers, and demand is growing for a workforce trained in this discipline. Downstream Recovery and Purification is an affordable, accessible desk reference on biomanufacturing for professionals, instructors, and students. With information on equipment, process and facility design, cGMP operation, and regulatory compliance, it is based on Wiley's 7-volume Encyclopedia of Industrial Biotechnology, Bioprocess, Bioseparation, and Cell Technology and features more than 50 carefully selected articles. Students and professionals alike will value this practical guide"-- |c Provided by publisher | ||
| 520 | |a "The 50 article reference work provides information on downstream recovery of cells and protein capture, process development and facility design, equipment, cGMP operations, and regulatory compliance"-- |c Provided by publisher | ||
| 504 | |a Includes bibliographical references and index. | ||
| 588 | 0 | |a Print version record. | |
| 505 | 0 | |a pt. I. Introduction -- pt. II. Downstream recovery of cells and protein capture -- pt. III. Process development in downstream purification -- pt. IV. Equipment design for downstream recovery and protein purification -- pt. V. Downstream cGMP operations -- pt. VI. Biopharmaceutical facility validation -- pt. VII. FDA cGMP regulatory compliance. | |
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| 700 | 1 | |a Flickinger, Michael C., |e editor. | |
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