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Vaccine Development and Manufacturing
  • Language: en
  • Pages: 452

Vaccine Development and Manufacturing

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 a...

Bioprocessing Technology for Production of Biopharmaceuticals and Bioproducts
  • Language: en
  • Pages: 288

Bioprocessing Technology for Production of Biopharmaceuticals and Bioproducts

Written for industrial and academic researchers and development scientists in the life sciences industry, Bioprocessing Technology for Production of Biopharmaceuticals and Bioproducts is a guide to the tools, approaches, and useful developments in bioprocessing. This important guide: • Summarizes state-of-the-art bioprocessing methods and reviews applications in life science industries • Includes illustrative case studies that review six milestone bio-products • Discuses a wide selection of host strain types and disruptive bioprocess technologies

Preparative Chromatography for Separation of Proteins
  • Language: en
  • Pages: 577

Preparative Chromatography for Separation of Proteins

Preparative Chromatography for Separation of Proteins addresses a wide range of modeling, techniques, strategies, and case studies of industrial separation of proteins and peptides. • Covers broad aspects of preparative chromatography with a unique combination of academic and industrial perspectives • Presents Combines modeling with compliantce useing of Quality-by-Design (QbD) approaches including modeling • Features a variety of chromatographic case studies not readily accessible to the general public • Represents an essential reference resource for academic, industrial, and pharmaceutical researchers

Disposable Bioprocessing Systems
  • Language: en
  • Pages: 323

Disposable Bioprocessing Systems

  • Type: Book
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  • Published: 2016-04-19
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  • Publisher: CRC Press

Written by a researcher with experience designing, establishing, and validating biological manufacturing facilities worldwide, this is the first comprehensive introduction to disposable systems for biological drug manufacturing. It reviews the current state of the industry; tackles questions about safety, costs, regulations, and waste disposal; and guides readers to choose disposable components that meet their needs. This practical manual covers disposable containers, mixing systems, bioreactors, connectors and transfers, controls and sensors, downstream processing systems, filling and finishing systems, and filters. The author also shares his predictions for the future, calling disposable bioprocessing technology a "game changer."

Single-Use Technology in Biopharmaceutical Manufacture
  • Language: en
  • Pages: 572

Single-Use Technology in Biopharmaceutical Manufacture

This book gives an overview of commonly-used disposables in the manufacture of biopharmaceuticals, their working principles, characteristics, engineering aspects, economics, and applications. With this information, readers will be able to come to an easier decision for or against disposable alternatives and to choose the appropriate system. The book is divided into two parts – the first is related to basic knowledge about disposable equipment; and the second discusses applications through case studies that illustrate manufacturing, quality assurance, and environmental influence.

GMP Audits in Pharmaceutical and Biotechnology Industries
  • Language: en
  • Pages: 474

GMP Audits in Pharmaceutical and Biotechnology Industries

  • Type: Book
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  • Published: 2024-06-28
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  • Publisher: CRC Press

The fact that good manufacturing practice (GMP) audits in the pharmaceutical and biotechnology industries have to be evaluated, and with very limited resources, has created a gap in this field. The lack of trained and qualified GMP auditors is on the rise in all organizations that are required to implement FDA, EMA, MHRA, WHO, TGA, and PIC/S regulations. This volume is an essential reference source for those organizations operating in the field of health and presents the basic knowledge needed to perform audits. The author also provides useful tips and a selection of samples about GMP audits that are indispensable for professionals and health inspectors working in industry and health authori...

The Dacca Gazette
  • Language: en
  • Pages: 538

The Dacca Gazette

  • Type: Book
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  • Published: 1962-10
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  • Publisher: Unknown

None

National Union Catalog
  • Language: en
  • Pages: 616

National Union Catalog

  • Type: Book
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  • Published: 1978
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  • Publisher: Unknown

Includes entries for maps and atlases.

Chemical Engineering Faculties
  • Language: en
  • Pages: 280

Chemical Engineering Faculties

  • Type: Book
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  • Published: 1987
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  • Publisher: Unknown

None

Dacca Law Cases
  • Language: en
  • Pages: 1140

Dacca Law Cases

  • Type: Book
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  • Published: 1971
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  • Publisher: Unknown

None