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国家药监局:2025年已批准上市18款生物制品 支持先进治疗药品研发
Zhong Zheng Wang·2025-09-19 10:25

Core Insights - The fifth China Biopharmaceutical Quality Control Conference highlighted the National Medical Products Administration's (NMPA) comprehensive reform of drug regulation, aimed at enhancing review and approval quality and efficiency, thereby stimulating innovation in the biopharmaceutical sector [1] Regulatory Developments - The NMPA plans to fully implement the State Council's opinions on deepening drug and medical device regulatory reforms to promote high-quality development in the pharmaceutical industry [1] - Future reforms will focus on improving the review and approval system, enhancing regulatory frameworks, and addressing clinical needs [1] Industry Growth - Among the 56 innovative drugs approved for market by 2025, 18 are biopharmaceutical products, indicating a significant presence of biopharmaceuticals in the innovation pipeline [1] - The NMPA aims to support the development of advanced therapeutic drugs and encourage companies to integrate into international innovation and supply chains, promoting high-quality growth in China's biopharmaceutical industry [1]