中药临床调剂技术规范化研究探讨  

Investigation on the standardization of Prescription Technology on Chinese clinical pharmacy

作　　者：翟华强[1] 高明超[1] 刘迪谦[1] 毛敏[2] 郑虎占[1] 

机构地区：[1]北京中医药大学中药学院,北京100102 [2]中日友好医院药学部,北京100029

出　　处：《中华中医药杂志》2010年第2期257-259,共3页China Journal of Traditional Chinese Medicine and Pharmacy

基　　金：国家"十一五"科技支撑计划子课题(No.2006BAI21B01);北京市"十一五"教育规划2009年度课题(No.CDA09050)~~

摘　　要：开展中药临床调剂技术规范化研究既是保障临床合理用药的要求,也是推动中医药行业标准化建设的重要一环。对中药临床调剂过程中处方审核、处方计价、处方应付、调配剂量、脚注执行、调剂复核、发药交待等7项技术环节进行规范化探讨,是健全和完善药学服务体系的有效方法。It is significant to carry out standardization of Prescription Technology on Chinese clinical pharmacy,which will not only improve the regulation of traditional Chinese medicine techniques,but also promote the standardization of the pharmaceutical industry an important part of the building. The discussion of seven areas of clinical medicine about Prescription audit, prescription pricing, prescription cope, deployment dose, footnote implementation, regulating review, dispensing explain for standardization will be improving and perfecting the pharmacy service system.

关 键 词：规范化研究 调剂技术 临床中药 

分 类 号：R283.3[医药卫生—中药学]