全球注册 | 韩国

你在韩国的许可持有人

作为在韩国的全球注册专家,我们确保您的产品符合韩国食品药品安全部 (MFDS) 的所有监管要求,助您成功进入韩国市场。

韩国许可持有人(KLH)

在韩国,必须具备一个韩国本地的注册地址或指定一位韩国许可持有人,以作为与韩国食品药品安全部 (MFDS) 的联络人。

根据不同的产品的分类,注册期限为2到16个月。对于I类产品,可以获得基本的KGMP证书。如果您的设备属于I类(特殊控制类)、II类、III类或IV类,则必须向MFDS提交详细的技术档案,并提供样品设备以进行测试。

CMC 可以通过在韩国食品药品安全部 (KFDA) 注册您的产品,帮助您进入韩国市场。

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    摘要
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    Frequently asked questions about TGA Registration

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    No, while the sponsor ensures that the products comply with Australian regulations and manages communication with the TGA, the foreign manufacturer is ultimately responsible for the quality and safety of their products.

    Yes, your distributor or any other individual/entity based in Australia can act as your TGA sponsor. However, it’s essential that they are qualified and willing to assume the regulatory responsibilities associated with this role.

    The cost varies depending on the sponsor’s services and the type of therapeutic goods being registered. It’s important to choose a reliable sponsor who can ensure compliance with TGA regulations.

    Without a TGA sponsor, your company cannot legally supply therapeutic goods in Australia. The sponsor is the official point of contact and is required for regulatory approval, ongoing compliance, and communication with the TGA.

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    Why appoint CMC Medical Devices as your TGA Sponsor?

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    Other Authorised Representative Services

    eu rep service
    UK representation service
    ch representation services
    fda rep service
    2025年9月12日新添加-结束