医疗器械在中国国家药品监督管理局(NMPA)的注册

CMC Medical Devices 提供医疗器械在中国的注册和审批服务

我们提供在中国的代理人服务,协助您的产品进入中国市场,并确保符合当地法规。我们确保符合中国的法规,并帮助您的医疗器械进入中国市场。

中国授权代表

CMC Medical Devices Shanghai Co., Ltd, 能够为在华无分支机构的境外制造商, 作为其 中国授权代表”,帮助其完成进口医疗器械产品在中国国家药品监督管理局的注册及相应监管和法规事务,提供全面的服务,确保您的产品符合国家药品监督管理局的NMPA的要求。

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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
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