An analysis on designation and marketing authorizations of orphan medicinal products from 2000 to 2015 in EULI Xuan, DU Xiao-chun, ZONG Xin2761-2765
Some important considerations on the evaluation of male reproductive toxicity for pharmaceuticals and introduction of FDA's related guidancesZHANG Li-jiang, HUANG Fang-hua, WANG Qing-li, ZHENG Gao-li2766-2772
Evaluation of the toxicity of vinorelbine bitartrate injectable emulsion and VRL aqueous injection in zebrafish张洪瑶, 贾飞, 钱璟, 劳乔聪, 刘洪翠, 李春启, 陶巧凤, 郭殿武2773-2779
International pharmacoeconomics review of erlotinib in the treatment of non-small cell lung cancerZHANG Dong, LI Xuan, LIU Yue-hua, ZHU Liu-bao2780-2786
Collection and analysis of the data of plants containing emodin-8-O-β-D-glucopyranoside in ChinaLI Kai-ming, SUN Zhen-xiao2787-2792
Ethics and rights protection of vulnerable group in clinical trials of drugs for dementia曾令烽, 刘军, 潘建科, 曹烨, 包文虎, 关梓桐, 朱黎婷, 曹倩, 李晓彦2793-2798
Preliminary discussion on safety evaluation of traditional Chinese medicine in early clinical researchLI Rui, CAO Wei-yi, TANG Xu-dong, SUN Ming-yue, LU Fang, GAO Rui2799-2803
Risk of clinical trials of innovative drugs and the protection of subjectsZHONG Jiao, WANG Li-ping2804-2806
Comparison of the expedited programs of patent drugs in China and America based on the empirical analysis of conditional approval systems for innovative drugsDING Jin-xi, LI Peng-hui, YAO Xue-fang2807-2813
Feasibility study on the implementation of patent linkage system in China——Based on analysis of stakeholdersYAO Xue-fang, ZHANG Guo-cheng, DING Jin-xi2814-2820