Analysis of the current status and trends in recombinant protein vaccine research and developmentXU Li, LI Huan, LIU Min, LI Xiao-jing, HE Wu2577-2584
Application of platform technology and regulatory considerations for innovative monoclonal antibody productsQIU Xiao, WANG Wen-bo, YANG Fei, ZHANG Meng-meng, GONG Xu, WEI Wei2585-2588
Advances in artificial intelligence-driven neoantigen prediction algorithmLI Qian, WANG Xue, JIN Xiang-wan-er, KOU Ya-zhen, HUANG Ying, HE Wu2589-2597
Quality risk management and considerations on evaluation of stem cell-derived pancreatic islet cell medicinal productsLIU Dan, LU Jia-qi, YIN Hui-fang, WEI Wei2598-2604
Pharmaceutical technical requirements and prospects for cell-based regenerative medicine therapeutic drugsHAN Dong-mei, DONG Jing, WEI Wei2605-2609
Analysis of common issues in quality control and evaluation of mesenchymal cell therapeutic drugsWEI Wei, CHENG Su-yuan, HAN Dong-mei, HE Wu2610-2615
Research progress and pharmaceutical considerations on therapeutic cancer vaccinesWANG Xue, LI Qian, YANG Fei, HE Wu2616-2621
CMC evaluation considerations for tumor-infiltrating lymphocyte in clinical trial applicationCUI Jing, WANG Xue, WEI Wei2622-2628
Post-approval CMC submissions and regulatory considerations for autologous CAR-T cell productsWANG Jing-yu, WANG Xue, LU Jia-qi, WEI Wei2629-2634