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美国食品药品监督管理局对医疗保健和生物医学领域人工智能监管的看法。

FDA Perspective on the Regulation of Artificial Intelligence in Health Care and Biomedicine.

作者信息

Warraich Haider J, Tazbaz Troy, Califf Robert M

机构信息

US Food and Drug Administration, Silver Spring, Maryland.

出版信息

JAMA. 2025 Jan 21;333(3):241-247. doi: 10.1001/jama.2024.21451.

Abstract

IMPORTANCE

Advances in artificial intelligence (AI) must be matched by efforts to better understand and evaluate how AI performs across health care and biomedicine as well as develop appropriate regulatory frameworks. This Special Communication reviews the history of the US Food and Drug Administration's (FDA) regulation of AI; presents potential uses of AI in medical product development, clinical research, and clinical care; and presents concepts that merit consideration as the regulatory system adapts to AI's unique challenges.

OBSERVATIONS

The FDA has authorized almost 1000 AI-enabled medical devices and has received hundreds of regulatory submissions for drugs that used AI in their discovery and development. Health AI regulation needs to be coordinated across all regulated industries, the US government, and with international organizations. Regulators will need to advance flexible mechanisms to keep up with the pace of change in AI across biomedicine and health care. Sponsors need to be transparent about and regulators need proficiency in evaluating the use of AI in premarket development. A life cycle management approach incorporating recurrent local postmarket performance monitoring should be central to health AI development. Special mechanisms to evaluate large language models and their uses are needed. Approaches are necessary to balance the needs of the entire spectrum of health ecosystem interests, from large firms to start-ups. The evaluation and regulatory system will need to focus on patient health outcomes to balance the use of AI for financial optimization for developers, payers, and health systems.

CONCLUSIONS AND RELEVANCE

Strong oversight by the FDA protects the long-term success of industries by focusing on evaluation to advance regulated technologies that improve health. The FDA will continue to play a central role in ensuring safe, effective, and trustworthy AI tools to improve the lives of patients and clinicians alike. However, all involved entities will need to attend to AI with the rigor this transformative technology merits.

摘要

重要性

人工智能(AI)的进步必须与努力相匹配,即更好地理解和评估AI在医疗保健和生物医学领域的表现,以及制定适当的监管框架。本专题通信回顾了美国食品药品监督管理局(FDA)对AI的监管历史;介绍了AI在医疗产品开发、临床研究和临床护理中的潜在用途;并提出了在监管系统适应AI独特挑战时值得考虑的概念。

观察结果

FDA已批准了近1000种使用AI的医疗设备,并收到了数百份关于在发现和开发过程中使用AI的药物的监管申报。健康AI监管需要在所有受监管行业、美国政府以及国际组织之间进行协调。监管机构需要推进灵活的机制,以跟上生物医学和医疗保健领域AI的变化步伐。申办者需要保持透明,监管机构需要精通评估AI在上市前开发中的使用情况。将经常性的本地上市后性能监测纳入其中的生命周期管理方法应成为健康AI开发的核心。需要特殊机制来评估大语言模型及其用途。有必要采取措施平衡从大公司到初创企业等整个健康生态系统利益相关者的需求。评估和监管系统需要关注患者健康结果,以平衡开发者、支付方和医疗系统为实现财务优化而使用AI的情况。

结论与意义

FDA的有力监督通过专注于评估以推进改善健康的受监管技术,保护了行业的长期成功。FDA将继续在确保安全、有效和值得信赖的AI工具以改善患者和临床医生生活方面发挥核心作用。然而,所有相关实体都需要以这种变革性技术应有的严谨态度对待AI。

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