摘要
本文以我国生物等效性研究相关指导原则为主要依据,参考国际先进监管机构相关要求,结合循环系统药物的特点,对循环系统药物口服固体制剂仿制药生物等效性研究给出几点考虑。
Drawing upon the relevant guidances on the bioequivalence study in China,referring to the requirements of international advanced supervision organization,considering the characteristics of the circulatory system drugs,this paper provides several considerations on the bioequivalence studies of the oral solid preparation generic drugs in the circulatory system.
作者
刘霏霏
闫方
宋晓
王骏
LIU Fei-fei;YAN Fang;SONG Xiao;WANG Jun(National Medical Products Administration Center for Drug Evaluation,Beijing 100076,China)
出处
《中国临床药理学杂志》
CAS
CSCD
北大核心
2024年第5期778-784,共7页
The Chinese Journal of Clinical Pharmacology
关键词
循环系统药物
口服固体制剂仿制药
生物等效性研究
circulatory system drugs
oral solid preparation generic drugs
bioequivalence studies