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Gunnar Eliasson: Handbook of Downstream Processing - nuovo libro
ISBN: 9789400915633
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?; PDF; Scientific, Technical and Medical > Biochemical engineering > Biotechnology, Springer Netherlands<
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E. Goldberg: Handbook of Downstream Processing - nuovo libro
ISBN: 9789400915633
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? Books > Chemistry eBook, Springer Shop<
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>100: Handbook of Downstream Processing - nuovo libro
ISBN: 9789400915633
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? SCIENCE,Biotechnology, eBooks.com<
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(*) Libro esaurito significa che il libro non è attualmente disponibile in una qualsiasi delle piattaforme associate che di ricerca.
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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Nr. 978-94-009-1563-3. Costi di spedizione:Worldwide free shipping, , DE. (EUR 0.00) Details...
(*) Libro esaurito significa che il libro non è attualmente disponibile in una qualsiasi delle piattaforme associate che di ricerca.
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?; PDF; Scientific, Technical and Medical > Biochemical engineering > Biotechnology, Springer Netherlands<
No. 9789400915633. Costi di spedizione:Instock, Despatched same working day before 3pm, zzgl. Versandkosten., Costi di spedizione aggiuntivi
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? Books > Chemistry eBook, Springer Shop<
new in stock. Costi di spedizione:zzgl. Versandkosten. (EUR 0.00)
>100: Handbook of Downstream Processing - nuovo libro
ISBN: 9789400915633
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? SCIENCE,Biotechnology, eBooks.com<
new in stock. Costi di spedizione:zzgl. Versandkosten., Costi di spedizione aggiuntivi
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<
Nr. 978-94-009-1563-3. Costi di spedizione:Worldwide free shipping, , DE. (EUR 0.00)
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Informazioni dettagliate del libro - Handbook of Downstream Processing
EAN (ISBN-13): 9789400915633 Anno di pubblicazione: 2012 Editore: Springer Netherlands
Libro nella banca dati dal 2017-02-25T13:09:58+01:00 (Zurich) Pagina di dettaglio ultima modifica in 2024-03-18T16:57:27+01:00 (Zurich) ISBN/EAN: 9789400915633
ISBN - Stili di scrittura alternativi: 978-94-009-1563-3 Stili di scrittura alternativi e concetti di ricerca simili: Autore del libro : jim goldberg
Dati dell'editore
Autore: E. Goldberg Titolo: Handbook of Downstream Processing Editore: Springer; Springer Netherland 720 Pagine Anno di pubblicazione: 2012-12-06 Dordrecht; NL Lingua: Inglese 309,23 € (DE) 317,90 € (AT) 354,00 CHF (CH) Available XXVIII, 720 p.
1 Mechanical disruption of cells.- 2 Conventional filtration.- 3 Pharmaceutical applications of liquid-liquid extraction.- 4 Affinity adsorption.- 5 Membrane separations in downstream processing.- 6 Electrodialysis.- 7 Large-scale column chromatography — a GMP manufacturing perspective.- 8 Product recovery and purification via precipitation and crystallization.- 9 Lyophilization.- 10 Drying in the pharmaceutical and biotechnology fields.- 11 Sterilization in the pharmaceutical and biotechnology industry.- 12 Pharmaceutical packaging operations.- 13 Clean-in-place and sterilize-in-place systems.- 14 Controls and automation for biotechnology and pharmaceutical industries.- 15 Agitation in fermenters and bioreactors.- 16 Distillation in the pharmaceutical industry.- 17 High purity water.- 18 The facility design process.- 19 Clean room testing and certification.- 20 Regulatory considerations.- 21 Validation.- 22 Project execution for the design and construction of a biotechnology facility.- 23 Bulk pharmaceutical and biopharmaceutical plant design considerations.- 24 Optimization of protein recovery using computer-aided process design tools.- 25 Off-site construction.- 26 Waste water treatment in the pharmaceutical industry.
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