摘要
本文概括性地介绍了美国FDA的《医疗器械ISO13485:2003自愿性审核报告提交程序》。结合FDA及其他国家和地区的监管部门对医疗器械制造商质量体系的检查,介绍了该程序的主要原则、适用情况;同时探讨了引入社会资源对医疗器械进行监管的科学、合理性,为我国医疗器械监管者在建立和修订我国的医疗器械法规时提供借鉴。
Brielfy introduce FDA Medical device ISO13485:2003 Voluntary audit report submission pilot program, combination with the quality system inspection of FDA and other regulatory affair, outlined the principle and application of this pilot program. And discuss that scientiifcity and rationality of introduce society resource to medical device supervision. Provide reference to our medical device supervisor when establish or revise China medical device regulation.
出处
《中国医疗器械信息》
2014年第8期44-48,共5页
China Medical Device Information
关键词
自愿提交
医疗器械
质量体系
审核报告
voluntary submit
medical device
quality system
audit report