摘要
目的规范国家药品标准物质协作标定的技术要求与管理程序,保证国家药品标准物质特性量值的准确性。方法详细介绍协作标定的技术要求与管理程序。结果与结论建立国家药品标准物质协作标定的技术要求与管理程序有助于协作标定参加实验室正确实施与理解药品标准物质的协作标定工作。
Objective To standardize the technical requirements and management procedures of collaborative calibration, so as to ensure the accuracy of the characteristic value of national pharmaceutical reference standards. Methods Technical requirements and management procedures of collaborative calibration were described in detail. Results and Conclusion The establishment of collaboration technical requirements and management procedures of national pharmaceutical reference standards collaborative calibration will benefit to the participating laboratories for the correct implementation of the work and understanding of the management procedures.
出处
《中国药事》
CAS
2012年第7期701-703,共3页
Chinese Pharmaceutical Affairs
基金
重大新药创制:国家科技重大新药创制"化学新药质量标准研究与评价技术平台"(编号2011ZX09303-001)
关键词
药品标准物质
协作标定
技术要求
管理程序
procedures pharmaceutical reference standards
collaboration
technical requirements
management
