我国妇幼专科医院药物临床试验机构发展现状分析OA
Analysis on the Development Status of Drug Clinical Trial Institutions in Maternal and Child Specialized Hospitals in China
目的 分析我国妇幼专科医院药物临床试验机构(以下简称妇幼专科GCP机构)现状.方法 查询国家药品监督管理局官网及药物临床试验相关平台,检索时限为 2005年 2月至 2019年 11月(资格认定期间)及 2019年 12月至 2024年 12月(备案制期间),统计和分析妇幼专科GCP机构的总体情况、地域分布、备案专业、主要研究者(PI)、承担药物临床试验总体情况、不同机构类型备案及承担试验情况、监督检查情况.结果 实施备案制后妇幼专科GCP机构数量由 42 家增至 94 家,全国 26 个省级行政区间的机构数量分布存在显著差异,且东部和中部地区集中趋势明显;共备案专业 678 个,以儿科专业(287 个,42.33%)及妇产科专业(123 个,18.14%)居多;备案PI共 1 395 人,承接药物临床试验共 3 282 项,且均以高校附属医院居多;不同机构类型备案及承担药物临床试验呈现明显的层级分化特征,备案机构数量以地市级医院为主(45 家,47.87%).累计接受监督检查 285 次,其中有因检查(92.31%)及日常监督检查(91.51%)的合规率较高,而注册核查合规率最低(72.22%).各省妇幼专科GCP机构年均监督检查 0.81 次/机构,省份间频次不均衡现象突出.结论 近 10 年,我国妇幼专科GCP机构专业聚焦度高,在特定领域具有显著的诊疗优势与患者集中度,但存在省份和区域分布不均、机构类型间备案与试验承担量层级分化明显的问题.建议通过政策激励、技术创新和妇幼专科联盟建设等途径优化妇幼药物临床试验资源配置,推动妇幼专科用药的研发.
Objective To analyze the current status of drug clinical trial institutions in maternal and child specialized hospitals(hereinafter referred to as maternal and child specialized GCP institutions)in China.Methods Data were retrieved from the official website of the National Medical Products Administration,and the platform,related to drug clinical trial institutions.The retrieval period covered from February 2005 to November 2019(during the qualification certification period)and from December 2019 to December 2024(during the filing system period).The overall situation,geographical distribution,filed specialties,principal investigators(PIs),the overall situation of undertaken drug clinical trials,filing and trial undertaking situations by different institution types,and supervision and inspection situations of maternal and child specialized GCP institutions were counted and analyzed.Results After the implementation of the filing system,the number of maternal and child specialized GCP institutions increased from 42 to 94.There were significant differences in the distribution of institution numbers among 26 provincial-level administrative regions,with a clear concentration trend in the eastern and central regions.A total of 678 specialties were filed,with the speciaty of pediatrics(287,42.33%)and the speciaty of obstetrics and gynecology(123,18.14%)accounting for the majority.A total of 1 395 PIs were filed,and 3 282 clinical drug trials were undertaken,most of which were completed by affiliated hospitals of universities.The filing and undertaking of clinical drug trials exhibited a clear hierarchical differentiation pattern by institution type,with municipal hospitals being the most common among filed institutions(45,47.87%).A total of 285 supervision and inspection activities were conducted.The compliance rates of cause-initiated inspection(92.31%)and routine supervision inspection(91.51%)were relatively high,while the compliance rate of registration inspection was the lowest(72.22%).The average annual number of supervision and inspection per maternal and child specialized GCP institution was 0.81,showing prominent imbalance among different provinces.Conclusion In the past decade,maternal and child specialized GCP institution in China have high professional concentration and possess outstanding clinical advantages and sufficient patient resources in targeted fields.Nevertheless,they are faced with uneven regional distribution and distinct hierarchical gaps in filing scale and trial undertaking capacity.It is suggested to optimize the allocation of drug clinical trial resources and promote the research and development of maternal and child specific medications through policy incentives,technical innovation and establishment of maternal and child specialized medical alliances.
张立段;彭丽艳;于庆坤
河北省唐山市妇幼保健院,河北 唐山 063000河北省唐山市妇幼保健院,河北 唐山 063000河北省唐山市妇幼保健院,河北 唐山 063000
医药卫生
妇幼专科医院药物临床试验机构备案药品监管
maternal and child specialized hospitaldrug clinical trialinstitutional filingdrug regulation
《中国药业》 2026 (12)
18-24,7
河北省中医药类科研计划课题[2019207].
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