E. Goldberg:Handbook of Downstream Processing
- copertina rigida, flessible 1996, ISBN: 0751403644
[EAN: 9780751403640], Neubuch, [PU: Springer Netherlands Okt 1996], DOWNSTREAMPROCESSING; FERMENTER; LYSIN; BIOCHEMICALENGINEERING; BIOTECHNOLOGY; CHROMATOGRAPHY; FILTRATION; MICROORGANIS… Altro …
[EAN: 9780751403640], Neubuch, [PU: Springer Netherlands Okt 1996], DOWNSTREAMPROCESSING; FERMENTER; LYSIN; BIOCHEMICALENGINEERING; BIOTECHNOLOGY; CHROMATOGRAPHY; FILTRATION; MICROORGANISM; PROTEIN; WASTEWATER, This item is printed on demand - it takes 3-4 days longer - Neuware -The last two decades have seen a phenomenal growth of the field of genetic or biochemical engineering and have witnessed the development and ultimately marketing of a variety of products-typically through the manipulation and growth of different types of microorganisms, followed by the recovery and purification of the associated products. The engineers and biotechnologists who are involved in the full-scale process design of such facilities must be familiar with the variety of unit operations and equipment and the applicable regulatory requirements. This book describes current commercial practice and will be useful to those engineers working in this field in the design, construction and operation of pharmaceutical and biotechnology plants. It will be of help to the chemical or pharmaceutical engineer who is developing a plant design and who faces issues such as: Should the process be batch or continuous or a combination of batch and continuous How should the optimum process design be developed Should one employ a new revolutionary separation which could be potentially difficult to validate or use accepted technology which involves less risk Should the process be run with ingredients formulated from water for injection, deionized water, or even filtered tap water Should any of the separations be run in cold rooms or in glycol jacketed lines to minimize microbial growth where sterilization is not possible Should the process equipment and lines be designed to be sterilized in-place, cleaned-in-place, or should every piece be broken down, cleaned and autoclaved after every turn 756 pp. Englisch, Books<
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E. Goldberg:Handbook of Downstream Processing
- nuovo libro ISBN: 9780751403640
[ED: Buch], [PU: Springer Netherlands], Neuware - The last two decades have seen a phenomenal growth of the field of genetic or biochemical engineering and have witnessed the development … Altro …
[ED: Buch], [PU: Springer Netherlands], Neuware - The last two decades have seen a phenomenal growth of the field of genetic or biochemical engineering and have witnessed the development and ultimately marketing of a variety of products-typically through the manipulation and growth of different types of microorganisms, followed by the recovery and purification of the associated products. The engineers and biotechnologists who are involved in the full-scale process design of such facilities must be familiar with the variety of unit operations and equipment and the applicable regulatory requirements. This book describes current commercial practice and will be useful to those engineers working in this field in the design, construction and operation of pharmaceutical and biotechnology plants. It will be of help to the chemical or pharmaceutical engineer who is developing a plant design and who faces issues such as: Should the process be batch or continuous or a combination of batch and continuous How should the optimum process design be developed Should one employ a new revolutionary separation which could be potentially difficult to validate or use accepted technology which involves less risk Should the process be run with ingredients formulated from water for injection, deionized water, or even filtered tap water Should any of the separations be run in cold rooms or in glycol jacketed lines to minimize microbial growth where sterilization is not possible Should the process equipment and lines be designed to be sterilized in-place, cleaned-in-place, or should every piece be broken down, cleaned and autoclaved after every turn - Besorgungstitel - vorauss. Lieferzeit 3-5 Tage., DE, [SC: 0.00], Neuware, gewerbliches Angebot, 241x160x45 mm, 756, [GW: 1285g], Banküberweisung, Offene Rechnung, Kreditkarte, PayPal, Offene Rechnung (Vorkasse vorbehalten), Internationaler Versand<
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E. Goldberg:Handbook of Downstream Processing
- copertina rigida, flessible 1996, ISBN: 0751403644
[EAN: 9780751403640], Neubuch, [SC: 0.0], [PU: Springer Netherlands], DOWNSTREAMPROCESSING; FERMENTER; LYSIN; BIOCHEMICALENGINEERING; BIOTECHNOLOGY; CHROMATOGRAPHY; FILTRATION; MICROORGAN… Altro …
[EAN: 9780751403640], Neubuch, [SC: 0.0], [PU: Springer Netherlands], DOWNSTREAMPROCESSING; FERMENTER; LYSIN; BIOCHEMICALENGINEERING; BIOTECHNOLOGY; CHROMATOGRAPHY; FILTRATION; MICROORGANISM; PROTEIN; WASTEWATER, Druck auf Anfrage Neuware - Printed after ordering - The last two decades have seen a phenomenal growth of the field of genetic or biochemical engineering and have witnessed the development and ultimately marketing of a variety of products-typically through the manipulation and growth of different types of microorganisms, followed by the recovery and purification of the associated products. The engineers and biotechnologists who are involved in the full-scale process design of such facilities must be familiar with the variety of unit operations and equipment and the applicable regulatory requirements. This book describes current commercial practice and will be useful to those engineers working in this field in the design, construction and operation of pharmaceutical and biotechnology plants. It will be of help to the chemical or pharmaceutical engineer who is developing a plant design and who faces issues such as: Should the process be batch or continuous or a combination of batch and continuous How should the optimum process design be developed Should one employ a new revolutionary separation which could be potentially difficult to validate or use accepted technology which involves less risk Should the process be run with ingredients formulated from water for injection, deionized water, or even filtered tap water Should any of the separations be run in cold rooms or in glycol jacketed lines to minimize microbial growth where sterilization is not possible Should the process equipment and lines be designed to be sterilized in-place, cleaned-in-place, or should every piece be broken down, cleaned and autoclaved after every turn, Books<
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Handbook of Downstream Processing
- nuovo libroISBN: 9780751403640
The last two decades have seen a phenomenal growth of the field of genetic or biochemical engineering and have witnessed the development and ultimately marketing of a variety of products-… Altro …
The last two decades have seen a phenomenal growth of the field of genetic or biochemical engineering and have witnessed the development and ultimately marketing of a variety of products-typically through the manipulation and growth of different types of microorganisms, followed by the recovery and purification of the associated products. The engineers and biotechnologists who are involved in the full-scale process design of such facilities must be familiar with the variety of unit operations and equipment and the applicable regulatory requirements. This book describes current commercial practice and will be useful to those engineers working in this field in the design, construction and operation of pharmaceutical and biotechnology plants. It will be of help to the chemical or pharmaceutical engineer who is developing a plant design and who faces issues such as: Should the process be batch or continuous or a combination of batch and continuous? How should the optimum process design be developed? Should one employ a new revolutionary separation which could be potentially difficult to validate or use accepted technology which involves less risk? Should the process be run with ingredients formulated from water for injection, deionized water, or even filtered tap water? Should any of the separations be run in cold rooms or in glycol jacketed lines to minimize microbial growth where sterilization is not possible? Should the process equipment and lines be designed to be sterilized in-place, cleaned-in-place, or should every piece be broken down, cleaned and autoclaved after every turn?, Springer<
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E. Goldberg:Handbook of Downstream Processing
- copertina rigida, flessible ISBN: 0751403644
Handbook of Downstream Processing ab 427.99 € als gebundene Ausgabe: Auflage 1997. Aus dem Bereich: Bücher, Wissenschaft, Biologie, Medien > Bücher, Springer Netherlands
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