中国IND申报流程及资料撰写要求全解析-药品研发 ...
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近年来，随着中国加入ICH（国际人用药品注册技术协调会）及政策对创新药研发的大力支持，国内IND（新药临床试验申请）申报数量显著增长。据CDE发布的2023及2024年度药品 ...,中国IND申报流程及资料撰写要求全解析,蒲公英 - 制药技术的传播者 GMP理论的实践者
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