人工智能用于药物研发领域的法律挑战与治理OA
Legal Challenges and Governance of Artificial Intelligence Applications in the Field of Drug Research and Development
目的 为构建符合我国国情的药物研发领域人工智能(AI)应用治理框架提供思路及参考.方法 总结AI在药物研发领域的应用场景及技术特征,分析应用中存在的法律挑战,并提出健全我国药物研发领域AI应用法律治理的对策建议.结果 当前,AI在药物研发领域的应用包括"基于结构的药物设计"等,应用领域包括"新药发现与设计"等,核心技术/方法包括"分析蛋白三维结构,预测药物-蛋白结合模式与亲和力"等,共 8 类;面临的法律挑战包括数据权属不明引发的合规性问题,药物临床试验当事人尊严和自主性的保护,药物上市后监测的公平性和透明性,以及针对多元责任主体的归责和问责机制.对此,可通过构建治理原则体系,探索法律框架完善路径,制定监管体系优化方案,加强人才队伍建设,开展国际经验的本土化实践等对策不断完善法律治理.结论 AI技术显著提升了药物研发效率,但技术迭代与法律规制的脱节引发了多重风险.为规范药物研发AI应用的流程,保证制药企业的数据完整、安全,保障临床试验相关当事人的权益,应进一步完善相关法律法规.
Objective To provide ideas and references for constructing a governance framework for artificial intelligence(AI)applications in the field of drug research and development that aligns with China's national conditions.Methods Application scenarios and technical characteristics of AI in the field of drug research and development were summarized,legal challenges existing in the application were analyzed,and countermeasures and suggestions for improving the legal governance of AI application in the field of drug research and development in China were proposed.Results Currently,AI applications in the field of drug research and development include ″structure-based drug design″,and its application include ″new drug discovery and design″,the core technologies/methods include ″analyzing protein three-dimensional structures,predicting drug-protein binding modes and affinities″,a total of eight categories.The legal challenges faced include compliance issues arising from unclear data ownership,protection of the dignity and autonomy of drug clinical trial participants,fairness and transparency of post-marketing drugs surveillance,as well as the attribution and accountability mechanisms for multiple responsible subjects.In response,legal governance can be continuously improved through measures such as constructing a system of governance principles,exploring paths for improving the legal framework,formulating optimization plans for the regulatory system,strengthening talent team building,and carrying out localized practices of international experience.Conclusion AI technology has significantly improved the efficiency of drug research and development.However,the disconnection between technological iteration and legal regulation has triggered multiple risks.Relevant laws and regulations should be further improved to standardize the process of AI application in drug research and development,ensure the integrity and security of data for pharmaceutical companies,and safeguard the rights and interests of parties involved in clinical trials.
秦华;于德志;张淳煕;黄鹏
山东省济南市食品药品检验检测中心,山东 济南 250102山东省青岛市食品药品检验研究院·国家药品监督管理局海洋中药质量研究与评价重点实验室,山东 青岛 266071西安信息职业大学,陕西 西安 710125山东省济南市食品药品检验检测中心,山东 济南 250102
医药卫生
药物研发人工智能法律法规治理框架
drug research and developmentartificial intelligencelaws and regulationsgovernance framework
《中国药业》 2026 (6)
26-30,5
山东省济南市法治研究课题[济法办发[2025]1号,济司通[2024]32号].
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