Clinical trials in Russia: Achieving excellence

被引:0
|
作者
Reznik, RS [1 ]
Ichim, TE [1 ]
Petrov, V [1 ]
Reznik, BN [1 ]
机构
[1] Vita Clin Res, Los Angeles, CA 90048 USA
关键词
clinical trials; medical devices; guidelines; FDA; US; Russia;
D O I
10.1117/12.634618
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The Russian population offers a unique opportunity for conducting clinical trials in general, and specifically in the area of Medical Devices. Although the regulatory framework for approval of clinical trials and eventual marketing registration is based on an American-style format, details of operating in the Russian framework are very different. Understanding and leveraging the unique characteristics of the Russian system on the patient side, the investigator side, and the regulatory side is important in extracting optimum value out of clinical trials in Russia. Having performed Medical Device research and clinical trials in Russia, the authors overview the present system and describe various strategies for working in this growing but still under-utilized clinical trials arena.
引用
收藏
页码:377 / 382
页数:6
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