[Forty years of construction and innovative development of scientific regulation system of traditional Chinese medicine in China].

Q3 Pharmacology, Toxicology and Pharmaceutics
Jun-Ning Zhao, Zhi-Shu Tang, Hua Hua, Rong Shao, Jiang-Yong Yu, Chang-Ming Yang, Shuang-Fei Cai, Quan-Mei Sun, Dong-Ying Li
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引用次数: 0

Abstract

Since the promulgation of the first Drug Administration Law of the People's Republic of China 40 years ago in 1984, China has undergone four main stages in the traditional Chinese medicine(TCM) regulation: the initial establishment of TCM regulation rules(1984-1997), the formation of a modern TCM regulatory system(1998-2014), the reform of the review and approval system for new TCM drugs(2015-2018), and the construction of a scientific regulation system for TCM(2019-2024). Over the past five years, a series of milestone achievements of TCM regulation in China have been achieved in the six aspects, including its strategic objectives and the establishment of a science-based regulatory system, the reform of the review and approval system for new TCM drugs, the optimization and improvement of the TCM standard system and its formation mechanism, comprehensive enhancement of regulatory capabilities for TCM safety, international harmonization of TCM regulation and its role in promoting innovation. Looking ahead, centered on advancing TCMRS to establish a sound regulatory framework tailored to the unique characteristics of TCM, TCM regulation will evolve into new reform patterns, advancing and extending across eight critical fronts, including the legal framework and policy architecture, the review and approval system for new TCM drugs, the quality standard and management system of TCM, the comprehensive quality & safety regulation and traceability system, the research and transformation system for TCMRS, AI-driven innovations in TCM regulation, the coordination between high-quality industrial development and high-level regulation, and the leadership in international cooperation and regulatory harmonization. In this way, a unique path for the development of modern TCM regulation with Chinese characteristics will be pioneered.

【中国中医药科学调控体系建设与创新发展四十年】。
自1984年颁布第一部《中华人民共和国药品管理法》以来,中国的中医药监管经历了四个主要阶段:初步建立中医药监管规则(1984-1997年)、形成现代中医药监管体系(1998-2014年)、改革中药新药审评审批制度(2015-2018年)、构建科学的中医药监管体系(2019-2024年)。五年来,中国中医药监管在战略目标和科学监管体系建设、中药新药审评审批制度改革、中医药标准体系及其形成机制优化完善、中医药安全监管能力全面提升、中医药安全管理能力全面提升等六个方面取得了一系列里程碑式成就。中医药法规的国际协调及其促进创新的作用。展望未来,中医药监管将围绕推进中医药管理体系建设,构建符合中医药特色的完善监管体系,形成改革新格局,在法律框架和政策体系、中药新药审评审批制度、中医药质量标准和管理体系、综合质量安全监管和追溯体系、中医药研究转化体系、人工智能驱动的中医药监管创新、高质量产业发展与高水平监管对接、国际合作与监管协调引领等。走出一条独具中国特色的现代中医药法规发展之路。
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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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