椎体成形球囊扩张导管注册申报重点及难点分析

      Analysis of Key Points and Difficulties in Registration Application of Inflatable Bone Expander

      • 摘要: 随着椎体成形球囊扩张导管在治疗骨质疏松性椎体压缩骨折中的优势逐渐凸显,该类产品注册申报量日益增多。根据国家药品监督管理局对注册申报资料的相关要求,结合椎体成形球囊扩张导管产品特点,对申请人提交的注册申报资料应重点关注的基本信息、产品性能研究、产品生产制造、临床评价以及产品说明书等方面的相关要求进行了分析总结。其中重点是申报资料的规范性,难点是研究资料的科学合理性。对下一步相关从业人员规范注册申报资料提供意见和建议,帮助其优化注册申报资料质量,提高注册申报效率。

         

        Abstract: With the advantages of inflatable bone expander in the treatment of osteoporotic vertebral compression fractures, the number of applications for registration of such products is increasing. Based on the characteristics of the medical device, this article analyzed and summarized the relevant requirements for the basic information, product performance research, product manufacturing, clinical evaluation, and product instructions that should be focused on the registration application dossiers, as well as comply with the requirements of CMDE. The focus of the registration application for Inflatable Bone Expander should be the standardization of the application dossiers, while the difficulty was the scientific rationality of the research data. Comments and suggestions are provided to relevant practitioners on standardization of registration application dossiers. It may help them to optimize the quality of registration application dossiers while improve the efficiency of registration applications.

         

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