| 注册
首页|期刊导航|中国食品药品监管|医疗器械大动物试验操作规范与实践指南:介入类产品临床前研究的应用与实践

医疗器械大动物试验操作规范与实践指南:介入类产品临床前研究的应用与实践

刘贻声 张广湘 黄炜瑜 梁锦源 卢忠 孔繁圃

中国食品药品监管Issue(3):28-41,14.
✕
中国食品药品监管Issue(3):28-41,14.DOI:10.3969/j.issn.1673-5390.2026.03.003

医疗器械大动物试验操作规范与实践指南:介入类产品临床前研究的应用与实践

Standard Operating Procedures and Practical Guidelines for Large Animal Studies in Medical Devices:Application and Practice in the Preclinical Research of Interventional Products

刘贻声 1张广湘 1黄炜瑜 1梁锦源 1卢忠 2孔繁圃3

作者信息

  • 1. 威科检测集团有限公司
  • 2. 中国药品监督管理研究会医疗器械监管研究专业委员会
  • 3. 清华大学医学院
  • 折叠

摘要

Abstract

Large animal studies serve as an indispensable scientific bridge for high-risk interventional medical devices transitioning from preclinical research to human clinical trials.Guided by China's regulatory framework,including the Guidelines for Registration Review of Animal Studies of Medical Devices,this paper systematically reviews the technical considerations and developmental trends of large animal studies in the preclinical evaluation of interventional medical devices.First,the suitability of pigs,sheep,dogs,and non-human primates is comparatively analyzed in terms of anatomical structure,physiological characteristics,and coagulation mechanisms,highlighting the broad applicability of porcine models in cardiovascular and neurointerventional evaluations.Second,the status of major disease models is reviewed,including acute peripheral arterial thrombosis and aspiration models,selective renal artery embolization models,atherosclerosis models,acute myocardial infarction models,calcific valvular disease models,and chronic heart failure models.The clinical predictive value of techniques such as autologous thrombus formation,chemical induction,and genetic modification is also compared.Furthermore,the paper emphasizes that experimental design should follow the principles of randomization and multi-time-point observations.An evaluation framework encompassing safety,efficacy,and operational performance is systematically summarized,along with corresponding pathological quantification standards.Finally,in response to current challenges such as model limitations,ethical constraints,and high costs,the paper discusses the potential of emerging technologies,including advanced imaging,artificial intelligence,computational modeling,and organ-on-a-chip systems,to enhance evaluation precision and ethical alignment.This study aims to provide a systematic and scientific technical reference for the R&D design and registration of interventional medical devices,thereby facilitating clinical translation and advancing precision regulation of high-risk devices in China.

关键词

大动物试验/介入类医疗器械/临床前研究/动物模型/安全性评估

Key words

large animal studies/interventional medical devices/preclinical research/animal models/safety evaluation

分类

医药卫生

引用本文复制引用

刘贻声,张广湘,黄炜瑜,梁锦源,卢忠,孔繁圃..医疗器械大动物试验操作规范与实践指南:介入类产品临床前研究的应用与实践[J].中国食品药品监管,2026,(3):28-41,14.

中国食品药品监管

1673-5390

访问量0
|
下载量0
段落导航相关论文