摘要
药物基因组学是当前一个热点话题。FDA于2013年发布了"临床药物基因组学指导原则:早期临床研究的上市前评价和对说明书的建议",本文介绍其中第IV部分基因组学的临床评价。我国还没有类似的指导原则,期待本文对我国这方面的研究和监管有益。
Pharmacogenomics is currently a hot topic.FDA issued "Guidance for Industry Clinical Pharmacogenomics:Premarket Evaluation in Early-Phase Clinical Studies and Recommendations for Labeling"in 2013.The article introduces its IV Clinical Evaluation of Pharmacogenomics.There is no similar guidance in our country.It is expected to benefit the research and supervision of our country in this respect.
出处
《中国临床药理学与治疗学》
CAS
CSCD
2015年第2期208-212,共5页
Chinese Journal of Clinical Pharmacology and Therapeutics