咨询 | MDR

我们协助您准备技术文档

我们的MDR咨询服务确保完全符合欧洲医疗器械法规MDR 2017/745。

欧洲医疗器械法规(MDR)

医疗器械技术文件,也称为技术文档,是包含有关医疗器械的所有技术信息的文档的集合。

文档完备的技术文件表明医疗器械符合适用的法规要求,例如欧洲医疗器械法规(MDR)。

符合标准的医疗器械技术文件对于在欧盟获得和维持该器械的市场授权至关重要。

医疗器械的技术文件是产品上市前获得批准的先决条件,但定制产品除外。

CMC将根据新的MDR 2017/745法规指导您完成医疗器械在CE 认证中的各个步骤,直至为您的设备加贴CE标志。

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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

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    UK representation service
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