約314件1ページ目

日本語のみで絞り込む

条件を指定して検索しています。すべての条件を解除する

  • 最終更新日:1週間以内
  • 23時間前 -In Vitro Diagnostic Regulation (IVDR) and its Key Points The In Vitro Diagnostic Regulation. Key Points 1.Scope and Definition 2.Risk Classification 3.

    5日前 -Comparison of the key differences between the MDR and IVDR in the EU In the fast-paced world of medical devices, staying updated on regulatory changes is ...

    1日前 -On May 21, 2024, MHRA announced a policy to recognize international medical device approvals from Australia, Canada, EU, and USA, easing UK market access ...

    2日前 -It concerns certifications and applications under the Medical Device/IVD Regulations (MDR/IVDR). ... S.4.1 ... This is shown by an example from the US, which is ...

    4日前 -Comprehensive QMS Software for Medical Devices. Medical device QMS software is a digital application designed to help medical device companies comply with ...

    4日前 -The SAWP is responsible for advice on marketing authorisation applications and the Member States represented at CTCG oversee clinical trial applications (CTA).

    1日前 -Agile and customized quality and compliance solutions from ProPharma ensure your product remains compliant during all development stages.

    1日前 -The IVD Accelerator Programme runs for 4 months and is structured in three blocks focused on three key areas of knowledge and capabilities in in vitro ...

    6日前 -Building IVDR-compliant panels for haematological disorders Diagnostic purpose of the IVDR conjugated antibodies. Building IVDR compliant panels for ...

    1日前 -テレビの買い換えのため、不要になりました。普段使いは別のカセットで、本カセットは保存用としていたため、使用実績はあまりありません。 フォーマット済、 ...