摘要
通过了解医疗器械上市前研究的局限性,分析了医疗器械不良事件产生的原因,浏览了国内外当前的管理制度,提出了医疗器械不良事件监测对监测制度建立的作用。
Article analysis on cause of side effect and accident of equipment and look through manage rules about national and oversea through knowing the study localization before coming into market, and pointing effect of supervising on side effect and accident of equipment on built rule.
出处
《中国医学装备》
2006年第7期47-48,共2页
China Medical Equipment
