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  • 2024/3/2 -Information not provided, or provided in the wrong format, may result in prolonged review time, delays, or termination of review. Signed on Behalf of the ...

    2024/1/25 -In August 2022, the MDCG endorsed a position paper on the transition to the MDR and IVDR and specifically on notified body capacity and availability of medical ...

    2023/10/18 -Using an auditable structure that includes Annex II headings as a format will provide significant benefits, especially in presentation to the notified body or, ...

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    2024/4/15 -テンプレートにはMDRとIVDRの両方が記載されていますが、今回は、以下の医療機器についてテンプレートが公開されました。 ・DSVG 01:心臓アブレーションデバイス・DSVG 02 ...

    2024/4/17 -IVDR is a more stringent set of regulations for IVDs in the EU and it replaces the IVDD guidelines. It determines the requirements for placing in vitro ...

    2023/10/5 -IVDR technical documentation checklist for in vitro diagnostic medical devices ; 3.4.1, Overview in tabular format of outsourced processes and name/address of ...

    2023/12/21 -... IVDR. They are drafted in collaboration with interested parties represented in the various groups and denominated by the following format: “MDCG Year-Number ...

    2024/3/4 -The technical documentation is required to be maintained throughout the device lifecycle and expected to be indexed using an aligned, structured format, as ...

    2023/12/14 -This article talks about an overview of assigning IVDR codes in conformity assessment applications to ensure safety and compliance market access of products ...

    2023/10/31 -an easily-readable plain-text format, such as an 'about' file, or included on the start-up screen; c) software lacking a user interface such as middleware ...