亚洲社会药学 ›› 2019, Vol. 14 ›› Issue (3): 87-91.

• •    下一篇

Regulation of Drug Clinical Trials in China: Course and Development Trend

Zhang Xu, Tian Lijuan*   

  1. School of Business Administration, Shenyang Pharmaceutical University, Shenyang 110016, China
  • 出版日期:2019-09-20 发布日期:2019-10-12

Regulation of Drug Clinical Trials in China: Course and Development Trend

Zhang Xu, Tian Lijuan*   

  1. School of Business Administration, Shenyang Pharmaceutical University, Shenyang 110016, China
  • Online:2019-09-20 Published:2019-10-12
  • Contact: Tian Lijuan (1973-), associate professor. Major research area: pharmaceutical law and drug policy. Tel: 024- 23986549, E-mail: tianlijuan_8@126.com E-mail:tianlijuan_8@126.com

摘要: Objective To provide a basis for future regulation reform of drug clinical trials in China in the context of the continuous deepening of drug regulation reform. Methods Literature review and regulation study were conducted to analyze the course and development trend of drug clinical trial regulation in China. Results and Conclusion It is found that the regulation system and the standardization for clinical trials in China are gradually improving, but there is still a gap compared with developed countries. In the future, the regulation authorities still need to further improve relevant regulations, clarify regulation responsibilities, and to improve the drug clinical trial review system to ensure the quality of clinical trials and the safety and effectiveness of listed drugs.

关键词: drug clinical trial, administration, development course

Abstract: Objective To provide a basis for future regulation reform of drug clinical trials in China in the context of the continuous deepening of drug regulation reform. Methods Literature review and regulation study were conducted to analyze the course and development trend of drug clinical trial regulation in China. Results and Conclusion It is found that the regulation system and the standardization for clinical trials in China are gradually improving, but there is still a gap compared with developed countries. In the future, the regulation authorities still need to further improve relevant regulations, clarify regulation responsibilities, and to improve the drug clinical trial review system to ensure the quality of clinical trials and the safety and effectiveness of listed drugs.

Key words: drug clinical trial, administration, development course