摘要
目的为医疗器械科学监管决策提供参考。方法对2009年医疗器械国家监督检验工作中遇到的样品、检验方法、检验依据的标准等问题进行分析讨论。结果与结论提出对国家抽验工作管理和注册产品标准管理的几点建议。
Objective To help the scientific decision-making for supervision of medical device.Methods The analysis was carried out on the samples and standards used in the testing for the state quality supervision of medical devices.Results and Conclusion A few suggestions were put forward for state quality supervision and management of the product standards of medical devices.
出处
《中国药事》
CAS
2010年第10期939-940,共2页
Chinese Pharmaceutical Affairs
关键词
医疗器械
标准
监督
medical device
standard
supervision
