摘要
针对医疗器械产品注册审评过程中临床试验的常见问题,对二类医疗器械临床试验的基本要点作一简单的阐述,指导研发企业正确地进行临床试验。
The study is aimed to the common phenomenon of clinical trials in the medical device product registration and evaluation process.The basic elements of the medical device（II） clinical trials will be described to guide R D companies for clinical trials.
出处
《临床医学工程》
2012年第7期1221-1222,共2页
Clinical Medicine & Engineering
关键词
医疗器械
临床试验
Medical devices
Clinical trial
