• 摘要: 为规范和促进浙江省治疗药物监测(therapeutic drug monitoring,TDM)工作,浙江省医院药事管理质控中心药学检测管理质控组在TDM室间质评工作的基础上,进一步形成临床药学实验室开展TDM工作的管理共识。本共识明确了浙江省开展TDM工作的实验室建设规范和环境布局要求,人员资质要求,以及TDM质量控制和生物安全管理要求,对推动浙江省TDM工作的规范化发展有重要的指导意义。

       

      Abstract: In order to standardize and promote the therapeutic drug monitoring(TDM) work in Zhejiang Province, the Pharmaceutical Testing Quality Control Team of Zhejiang Provincial Hospital Pharmaceutical Management Quality Control Center further formed the management consensus of clinical pharmacy laboratory to carry out TDM work on the basis of TDM inter-laboratory quality assessment. The consensus defines the requirements of laboratory construction norms, environmental layout, personnel qualifications, TDM quality control, and biosafety management for TDM work in Zhejiang Province. The consensus has important guiding significance to promote the standardization development of TDM work in Zhejiang Province.

       

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