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Difficulties and countermeasures for the international acceptance of clinical trial data in ChinaSUN Yi-bu, HAO Zi-ruo, CHEN Yu-wen2486-2489
From FDA Complete Response Letters on the pharmaceutical assessment of chemical drugs:critical deficiencies and review considerationsREN Feng, CHENG Si-qi, JIANG Tao, CHEN Ai-ping, TANG Zhi-quan, ZHANG Jing-chen2490-2496
A multidisciplinary review of a new drug from the perspective of FDA Complete Response Letters and review reports:a case study of risperidone microspheresCHENG Si-qi, JIANG Tao, CHEN Ai-ping, TANG Zhi-quan, ZHANG Jing-chen, REN Feng2497-2501
Discussion on clinical pharmacology of novel anti-obesity drugs:glucagon-like peptide-1 receptor agonistsWANG Jing, LI Li, WEI Chun-min2502-2507
Research and application progress of biomarkers for Alzheimer's diseaseZHANG Shi-ye, QI Mei, GU Zhi-rong, GE Bin2508-2516
Application of minimal clinically important difference in economic evaluationLI Yan, HU Hong-fei, ZHAO Min, WANG Di, GAO Wei, LI Hong-chao2517-2525
Construction of breaking the blind risk assessment content for investigator test site in double-blind clinical trials of traditional Chinese medicine and suggestions for maintenance of blinding in clinical trialsYANG Fang-fang, PAN Ding-ju2526-2530