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Titlebook: Cell Therapy; cGMP Facilities and Adrian Gee Book 2009 Springer-Verlag US 2009 cancer.cell.gene.gene therapy.genes.regulation.research.ste

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11#
發(fā)表于 2025-3-23 10:51:22 | 只看該作者
12#
發(fā)表于 2025-3-23 16:59:20 | 只看該作者
Cleaning Proceduresres the development and implementation appropriate and effective methods for cleaning, procedures to monitor if these methods are indeed effective, and documentation of cleaning procedures on an ongoing basis. This chapter discusses various approaches that can be used to fulfill these requirements i
13#
發(fā)表于 2025-3-23 18:13:07 | 只看該作者
14#
發(fā)表于 2025-3-23 23:48:51 | 只看該作者
Supply Managementand cellular therapy products. In addition, a controlled and auditable procedure for the management of supplies and reagents is essential to provide traceability, and to ensure that products are manufactured using safe and appropriate components. This chapter describes procedures for developing and
15#
發(fā)表于 2025-3-24 06:15:41 | 只看該作者
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發(fā)表于 2025-3-24 07:03:46 | 只看該作者
https://doi.org/10.1007/b102110cancer; cell; gene; gene therapy; genes; regulation; research; stem cell; tissue
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發(fā)表于 2025-3-24 12:53:28 | 只看該作者
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發(fā)表于 2025-3-24 17:20:17 | 只看該作者
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發(fā)表于 2025-3-24 20:01:25 | 只看該作者
Cleaning Proceduresres the development and implementation appropriate and effective methods for cleaning, procedures to monitor if these methods are indeed effective, and documentation of cleaning procedures on an ongoing basis. This chapter discusses various approaches that can be used to fulfill these requirements in different types of cell processing facilities.
20#
發(fā)表于 2025-3-25 02:49:32 | 只看該作者
Supply Managementand cellular therapy products. In addition, a controlled and auditable procedure for the management of supplies and reagents is essential to provide traceability, and to ensure that products are manufactured using safe and appropriate components. This chapter describes procedures for developing and implementing a supply management system.
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