摘要
目的保证制剂质量,保障人体用药安全有效。方法对医疗机构制剂监督检查时发现的问题进行归纳。结果与结论药品监督管理部门应加大对医疗机构制剂的监管力度,促进医疗机构制剂室、药品检验室设施设备、质量标准、管理制度等不断完善。
Objective To ensure the quality of preparations and protect the people safe and effective medication.Methods The issues found in the supervision and inspection of preparations in medical institutions were summed up.Results and Conclusion The pharmaceutical supervision and management departments to intensify supervision of preparation in medical institutions,in order to promote preparation rooms for medical institutions,pharmaceutical testing laboratory facilities and equipment,quality standards,management system continuously to improve.
出处
《中国药事》
CAS
2010年第1期69-70,共2页
Chinese Pharmaceutical Affairs
关键词
医院制剂
药品监管
制剂室
hospital preparations
drug administration
preparation room
