Israel is a small country with significant medical device needs. Medical devices in Israel are regulated by AMAR and the registration process relies on your device's market authorization in other key markets. However, you still need to complete some key steps and meet requirements before putting your device on the Israeli market. In this short video, we'll give you an overview of what it takes you start selling your medical device in Israel. You will learn:
Emergo has the expertise and the local presence in Israel to help you expand your market reach.
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:
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