美国 | FDA代理

我们是您在美国的FDA代理

我们确保您的医疗器械符合FDA法规,确保快速安全地进入美国市场。

在CMC,我们协助没有美国总部的医疗器械和IVD制造商,作为他们的FDA独家代理。 我们在整个监管过程中提供专家指导,并作为您公司与FDA之间的联络点。

CMC提供全面的 FDA注册流程协助,确保您的产品符合所有法规标准。

510(K)

如果您需要在美国提交510(k)申请,CMC可以帮助您。我们专门指导医疗器械制造商通过向FDA提交流程。

美国FSC

CMC可以针对全球任何国家申请美国FSC(自由销售证书),包括每个国家特定的认证。
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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
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