摘要
本文介绍了《医疗器械生产质量管理规范(试行)》的实施范围、步骤、意义,对理解上的难点进行了深入解读,并针对企业给予了实施建议。
The arctical introduced the reference,procedure and significance implementation for good manufacturing practice for medical apparatus and instruments（for trial implementation）,interpreted the difficulties of understanding it,and afforded an assume for manufacturing enterprise about it.
出处
《中国医疗器械信息》
2010年第9期38-39,共2页
China Medical Device Information
关键词
医疗器械生产质量管理规范
实施
解读
good manufacturing practice for medical apparatus and instruments
implementation
interpretation
