With over 1.3 billion residents, China has one of the world's largest medical device markets. Medical device manufacturers around the world are intrigued by sales opportunities in China, but the regulatory process can be challenging. Interested in learning how to tap into this market? This short video tells you how.
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You may also like our free regulatory chart on the steps to regulatory approval in China.
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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