医疗器械临床试验质量控制问题分析与探讨

      Analysis and Discussion of Problems Founded in Quality Control of Medical Device Clinical Trials

      • 摘要: 对该院2016—2021年医疗器械临床试验机构层面质控发现的49项问题进行总结,从临床试验参与各方的角度分析问题产生的原因,探讨包括完善管理体系,加强研究者培训和优化研究者选择制度,强化申办者的职责和法规意识,制订申办者的选择依据等改进措施,保障临床试验质量,以期为临床试验管理者和实施者提供参考。

         

        Abstract: The quality control problems of 49 institutional level medical device clinical trials in hospital from 2016 to 2021 were summarized, and the causes of the problems were analyzed from the perspective of all parties involved in the clinical trial. The improvement measures were discussed, which including improving the management system, strengthening the training of researchers and optimizing the selection method, strengthening the responsibility and regulation consciousness of applicants, and formulating the selection basis of applicants and so on. All the above aims to ensure the quality of clinical trials and provide reference for clinical trial managers and implementers.

         

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