• 中国核心期刊(遴选)数据库收录期刊
  • 中文科技期刊数据库收录期刊
  • 中国期刊全文数据库收录期刊
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中国药物评价 ›› 2025, Vol. 42 ›› Issue (3): 166-171.

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医疗器械临床试验机构项目管理的思考及实践

 莫霞, 李瑶   

  1. 广东省妇幼保健院, 广东 广州 510010
  • 收稿日期:2025-03-17 修回日期:2025-04-23 接受日期:2025-08-05 出版日期:2025-06-28 发布日期:2025-08-05

Practice and Thinking Based on the Key Points of Project Management in Medical Device Clinical Trial Institutions

  MO Xia, LI Yao   

  1. Guangdong Women and Children Hospital, Guangdong Guangzhou 510010, China
  • Received:2025-03-17 Revised:2025-04-23 Accepted:2025-08-05 Online:2025-06-28 Published:2025-08-05

摘要:  医疗器械临床试验是验证拟上市注册医疗器械产品在其正常使用条件下安全性、有效性的关键环节,医疗器械临床试验需在备案的医疗机构中开展,医疗器械临床试验机构作为负责沟通协调、组织实施、监管培训、发展规划的管理部门,基于医疗器械临床试验流程,需做好医疗器械临床试验项目受理及推荐、项目立项评估、项目合同审查、项目启动及实施、医疗器械管理、样本管理、项目质控管理、项目经费管理、项目结题管理、项目档案管理、配合项目相关检查等各项工作,本文通过总结管理实践,分析以上医疗器械临床试验项目流程管理要点,可知医疗器械临床试验机构需要积极采取精细、专业、高效的管理流程,通过有效整合资源、积极沟通协调、快速响应需求、优化服务流程、严格风险管理,才能保证医疗器械临床试验过程规范、科学,助力医疗器械临床试验高质量发展,切实保障和落实医疗器械临床试验申办方、机构、研究者、受试者等相关方的各方权益及需求。

关键词: font-size:medium, ">医疗器械临床试验;临床试验机构;项目流程管理;规范化

Abstract: Clinical trial of medical device is the key link to verify the safety and effectiveness of medical device products to be listed and registered under normal conditions of use,Clinical trials of medical devices shall be carried out in registered medical institutions,The medical device clinical trial institution is the medical device clinical trial management department responsible for communication and coordination, organization and implementation, supervision and training, and development planning,based on the clinical trial process of medical devices,It is necessary to assist in project acceptance and recommendation, project evaluation, project contract review, project start-up and implementation, medical device management, sample management, project quality control management, project fund management, project closure management, project file management, and project related inspection and other work.This article summarizes management practices,and analyzes the key points of process management for the above-mentioned clinical trial projects of medical device.It can be known that medical device clinical trial institutions need to actively adopt fine, professional and efficient management processes, through effective integration of resources, active communication and coordination, rapid response to needs, optimization of service processes, and strict risk management, in order to ensure that the medical device clinical trial process is real and standardized, and the results are scientific and reliable. To support the high-quality development of medical device clinical trial, and effectively safeguard and implement the rights and demands of all relevant parties, including sponsors, institutions, researchers, and subjects.Effectively safeguard and implement the rights and demands of all relevant parties involved in medical device clinical trials, including sponsors, institutions, researchers, and subjects.

Key words: font-size:medium, ">Clinical trials of medical device; Clinical trial institution

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