全球注册 | 印度

您在印度的授权代表

我们为您提供在印度的全球注册服务,确保您的产品符合印度中央药品标准控制组织 (CDSCO) 的所有监管要求,以便您的产品高效且合规地进入印度市场。

印度授权代理人

制造商必须指定一名印度授权代理人来处理注册流程。

所有医疗产品的注册期限为6到9个月。印度的注册流程要求提交详细的技术文件。获得原产国批准(如FDA或CE)的制造商可以用其促进设备在印度的注册。注册证书的有效期为3年,必须在有效期届满前的6到9个月内重新申请。

CMC 可以在印度中央药品标准控制组织 (CDSCO) 注册您的产品,帮助您进入印度市场。

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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
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