Analysis of the Current Clinical Research Management System of Investigator Initiated Trials in China

Ye Cao, X. Wang, Yu Cao, Fuyu Song, S. Minelli, Jibin Li, Kexin Li, M. Hong
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Abstract

Objective: With the rapid increasing clinical trials in China in recent years, there has been rising concern on the management of investigator initiated trials. Compared with the trials sponsored by pharmaceutical companies, IIT is facing practical challenges in China due to the lack of experience by investigator and immature regulatory circumstances. We conducted an internet-based survey to understand the overall picture of IITs management in China. Methods: An internet-based questionnaire was developed and the staff of clinical trial offices from different types of hospitals was invited to provide response via mobile based App or online website in 2 weeks. We have collected the responses from the following aspects: administrative and governance infrastructure, ethical review, project management, funding resources and research staff management. Results: From December 8 to 20, 2016, a total of 259 responses were collected from the staffs that are mainly responsible for the clinical trial management and scientific research based in the different clinical facilities. Conclusion: In China, three key factors are important to improve the management on IITs: funding support, staffing resourcing and regulatory guidance.
中国研究者发起试验临床研究管理制度分析
目的:近年来,随着中国临床试验的快速增加,研究者发起试验的管理问题日益受到关注。与制药公司赞助的试验相比,由于研究者缺乏经验和监管环境不成熟,IIT在中国面临着现实挑战。我们进行了一项基于互联网的调查,以了解中国iit管理的总体情况。方法:制作网络问卷,邀请不同类型医院临床试验办公室的工作人员在2周内通过手机App或在线网站进行回答。我们收集了以下方面的回应:行政和管治基础设施、伦理审查、项目管理、资助资源和研究人员管理。结果:2016年12月8日至20日,在不同临床机构主要负责临床试验管理和科研的工作人员中,共收集到259份回复。结论:在中国,资金支持、人员配备和监管指导是改善iit管理的三个关键因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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