Japan is the second largest medical device market, representing about 10% of the world total. While the population of Japan continues to decline, the potential for medical device manufacturers continues to be promising. Why? Japan has a rapidly aging population and those people are much larger consumers of healthcare than younger citizens. But this potentially lucrative market has what may be one of the most complicated registration processes in the world.
We'll explain the Japanese approval process step by step in this free video. Once you begin the series you may skip to the next section at any time using the Playlist in the player window. Information current as of March 2015.
In this slidecast:
我们的专家将详细解读2023年韩国食品药品安全部(MFDS)指导文件草案更新下韩国医疗器械注册监管要求、分类标准、韩国良好生产规范(KGMP)等相关要求,并将依据多年韩国本地注册经验提供注册案例分享。此外,您还将了解到制造商在面对MFDS监管时需要关注的核心要点,相关研讨会内容包括:
阅读更多医疗器械和体外诊断(IVD)器械制造商需要在COFEPRIS注册他们的产品,COFEPRIS是墨西哥卫生部(Secretaría de Salud)的一个机构。器械在上市前需要上市前审批,豁免的器械除外。
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