咨询| ISO 13485

我们协助您建立质量管理体系

我们的ISO 13485咨询服务可帮助您实施和维护高效的医疗器械质量管理体系,确保符合国际标准。

按照ISO 13485进行质量管理

在CMC,我们可以帮助您根据ISO 13485:2016建立质量管理体系。

随着要求更严格的新法规生效,这一点尤为重要。我们的认证审核员将帮助您提高公司的质量。

2025年9月12日新添加
2025年9月12日新添加-联系我们表单提交

请填写联系表格,我们的顾问会尽快与您联系。

在世界各地找到我们

    后台栏目
    摘要
    2025年9月12日新添加-2

    Frequently asked questions about TGA Registration

    2025年9月12日新添加-3

    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.

    2025年9月12日新添加-4

    Why appoint CMC Medical Devices as your TGA Sponsor?

    2025年9月12日新添加-5

    Other Authorised Representative Services

    eu rep service
    UK representation service
    ch representation services
    fda rep service
    2025年9月12日新添加-结束