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:
自2018年起,美国食品和药物管理局(U.S. Food and Drug Administration,FDA)开始试行以电子化方式来帮助行业提供完整的510(k)上市前通知。2022年,为推进以电子格式提供510(k)递交文件的过渡,美国FDA正式发布关于使用电子递交模板和资源的最终指导文
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