High Cell Density and Perfusion Process Solutions
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Implementation and Optimization of Continuous Perfusion
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温度分布验证相关考虑
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湿热灭菌的科学原理
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计算机化系统GMP要求
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Bioreactor discussion
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QA人员现场管理
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实验室记录与数据管理
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GMP物料管理系统
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包材相容性密封性
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公用工程系统GMP合规性
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基因治疗药物的CMC开发策略
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洁净厂房施工与验收标准
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生物制药质量管理
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High-Quality Plasmid DNA Manufacturing Strategies for Gene and Cell Therapeutics
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Industrialization of Cell Therapy Manufacturing
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中国药典2020版分析方法验证通则解读
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洁净室物品GMP管理要求
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细胞库GMP管理要求
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生物制药的GMP检查要求
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ICH Q14分析方法开发指南解析
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稳定性试验的条件和具体实施要点和要求
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A cGMP Compatible, Non-Viral CAR T Cell Manufacturing Process
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Lentivirus vector manufacturing using suspension cell line
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VHP气相灭菌技术
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GMP附录-细胞治疗产品解读
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Utilizing the Gibco CTS Rotea System for cell and gene therapy development
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消毒技术
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All you need for T cell research
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Stem Cell Therapie's Potential in the Pandemic Era
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EU GMP Annex 1 Update_ Implications for Sterile Products Manufacture
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药品技术转移的法规要求和关键点分析
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Simplifying GMP CAR T and CAR NK cell therapy manufacturing processes
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How cell and gene therapies can transform the treatment of solid tumours
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CAR-T细胞产品IND申报CMC经验分享
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2022 WMIF，The Cell Therapy Landscape，CAR-T to Stem Cells
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FT596_ iPSC-derived CAR-NK cells with engineered persistence for B-cell malignan
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Natural Killer (NK) Cells Defenders Against Cancer
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生物制品GMP检查要点及常见缺陷
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CAR-T Cell Therapy_ Now and in 2030
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临床试验用药品GMP附录最新解析