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Titlebook: Cell Therapy; cGMP Facilities and Adrian P. Gee Book 2022Latest edition Springer Nature Switzerland AG 2022 cell processing facilities.cel

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發(fā)表于 2025-3-25 07:22:48 | 只看該作者
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發(fā)表于 2025-3-25 09:47:02 | 只看該作者
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發(fā)表于 2025-3-25 15:08:20 | 只看該作者
R. A. Klemm,P. A. Lee,T. M. RiceQuality control of cellular therapy products is an essential component of determining their safety and efficacy. This chapter reviews the various components of quality control testing of both cellular therapy products and viral vectors.
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發(fā)表于 2025-3-25 18:23:15 | 只看該作者
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發(fā)表于 2025-3-25 22:44:01 | 只看該作者
Quality Control of Cellular Therapy Products and Viral VectorsQuality control of cellular therapy products is an essential component of determining their safety and efficacy. This chapter reviews the various components of quality control testing of both cellular therapy products and viral vectors.
26#
發(fā)表于 2025-3-26 00:13:16 | 只看該作者
Introduction: Facility DesignThis chapter provides an introduction to the design of current good manufacturing (cGMP)/good tissue practices (cGTP) facilities in academic institutions. It is followed by separate chapters that provide information on a number of such facilities. In addition, there are chapters on cord blood banks and on a vector production facility.
27#
發(fā)表于 2025-3-26 08:13:48 | 只看該作者
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發(fā)表于 2025-3-26 12:01:13 | 只看該作者
Selection of Contract Manufacturing and Testing Organizationsd-alone hospital, wishes to build a cell processing facility to provide the products. An alternative is to use commercial companies for cell processing and/or testing. In recent years, a number of such entities have appeared, and this chapter addresses some of the factors that are involved in selecting those which can meet your needs.
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發(fā)表于 2025-3-26 12:54:02 | 只看該作者
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