期刊文献+

贵州省医疗机构制剂现况调查与分析 被引量:3

Investigation and Analysis of Pharmaceutical Preparations in Medical Institutions in Guizhou Province
下载PDF
导出
摘要 目的为了医疗机构制剂(简称"制剂")的可持续发展,调查研究制剂的发展现况。方法对2001~2015年制剂进行回顾性调查,深入分析制约发展的因素,为提出对策及建议提供科学依据。结果制剂在发展中存在的问题有:具有制剂许可证的医疗机构呈等级集中分布的趋势;仅多数三甲医院能生产制剂;多数医疗机构偏向于生产化学制剂;医疗机构对制剂注册要求不了解。依据调查结果。结论未来应结合贵州民族特色,重点研发中药制剂;药监部门出台相关政策鼓励创新;利用大数据发展优势,建立网络信息交流管理系统。 Objective: in order to achieve sustainable development of pharmaceutical preparations in medical institutions. Method: a retrospective investigation was conducted on the pharmaceutical preparations in medical institutions from 2001 to 2015 by investigating the current situation of pharmaceutical preparations in medical institutions in Guizhou province, and the factors restricting development were analyzed in depth, so as to provide scientific basis for countermeasures and suggestions. Results: there are some problems in the development of pharmaceutical preparations in medical institutions in Guizhou province: only most grade A hospitals can produce preparations;most medical institutions prefer to produce chemical agents;medical institutions are not aware of the requirements for preparation registration. Conclusion: according to the survey results, in the future, we should focus on the research and development of traditional Chinese medicine in combination with Guizhou’s ethnic characteristics;the drug regulatory department issued relevant policies to encourage innovation;use big data development advantage, establish network information exchange management system.
作者 张志宇 童红 李克林 Zhang Zhiyu;Tong Hong;Li Kelin(Inspection Center of Guizhou Medical Products Administration,Guiyang 550001,China)
出处 《广东化工》 CAS 2020年第16期98-99,共2页 Guangdong Chemical Industry
基金 黔科合基础[2016]1532-2。
关键词 医疗机构制剂 制剂现况 调查分析 调查制约因素 发展对策 pharmaceutical preparations in medical institutions preparation conditions investigation and analysis survey factors development countermeasures
  • 相关文献

参考文献4

二级参考文献5

  • 1国家食品药品监督管理局.《药品注册管理办法》[Z].北京:国家食品药品监督管理局局令第28号,2007.
  • 2国家药品监督管理局.《新药审批办法》[Z].北京:国家药品监督管理局局令第2号,1999.
  • 3国家药品监督管理局.《药品注册管理办法》(试行)[Z].北京:国家药品监督管珲局局令第35号,2002.
  • 4国家食品药品监督管理局.《药品注册管理办法》[Z].北京:国家食品药品监督管理局局令第17号,2005.
  • 5王宝新,杨小雷.试论医院制剂的现状与未来[J].中国药事,2000,14(1):28-30. 被引量:14

共引文献25

同被引文献63

引证文献3

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部