摘要
随着药品临床实验管理国际统一标准的逐步形成，我国逐步建立了药品监督管理体系和临床实验机构，开始进行规范的药品临床实验。本文对北京的临床药理基地进行了系统调研，找出阻碍临床试验发展的问题，并提出促进北京医药产品临床试验发展的对策与措施。
With the international standardization for drugs and clinical trials, China established its management system to supervise the institutions that carry out drug tests and clinical trials. This article presents a systematic research of Beijing Clinical Pharmacological Center, to explore existing problems in clinical trials and propose strategies and measures to cope with these problems, thus facilitate the development of clinical drug trials in Beijing.
出处
《中华医学科研管理杂志》
2011年第4期224-225,231,共3页
Chinese Journal of Medical Science Research Management
基金
北京市科技计划项目《北京临床研发服务能力提升的需求分析与技术选择》（Z08000704000805）
关键词
药物临床试验
监督管理
Drug clinical trials
Supervise institutions
