俄罗斯联邦药品本地化的一些具体监管方面和细微差别

Anna Soltitskaya
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摘要

关于俄罗斯的药品本地化规定,你应该知道一些重要的事情。对你们药品本地化项目有影响的主要地方法规和实际执法实践的简要概述。根据2015年11月30日俄罗斯政府法令№1289“关于外国制造商作为政府采购参与者生产的药品的限制”(所谓的规则“第三轮”):如果至少提交了两份俄罗斯产品的申请,那么来自某些外国制造商(不是俄罗斯产品)的任何第三份申请都不能被接受。俄罗斯联邦法61 FZ“药品流通”是规范药品(DP和API)流通(研发,临床试验,制造,专业知识和注册,供应,销售,营销等)的基本一般立法法案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Some Specific Regulatory Aspects and Nuances of Drug Products Localization in the Russian Federation
Some important things you should know about drug products localization regulations in Russia. Brief overview of the main local regulations and factual law-enforcement practices that have an impact on your drug products localization projects. According to the Russian Government Decree, № 1289 dated by Nov. 30, 2015 “On limitations of drug products manufactured by foreign manufacturers as participants of Government Procurement” (so called rule “The third wheel”): if two applications at least for the Russian products are submitted, so any third application from some foreign manufacturer (not the Russian product) cannot be accepted. The Russian Federal Law 61 FZ “On drugs circulation” is the basic general legislation Act that regulates Drugs (DP & API) circulation (research & developing, clinical trials, manufacturing, expertise and registration, supply, sale, marketing etc.)
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