授权代表 | 个人防护装备

您的个人防护装备授权代表

我们提供个人防护装备 (PPE) 的授权代表服务和合规支持,确保您顺利进入欧洲市场。

个人防护装备在欧盟的销售

个人防护装备的部署受PPE法规(EU) 2016/425的监管。该法规规定了非欧盟的个人防护设备进入欧盟市场的条件,并要求非欧盟的制造商必须指定一名欧洲授权代表 (EC-REP), 以帮助您的产品投放到欧盟市场。

CMC可以担任您的个人防护装备(PPE) 的授权代表,并作为您与主管当局的联络人。

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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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