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2 new MDCG documents issued: MDCG 2022-17 and MDCG 2022-18,
in Uncategorized
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Two Commission Implementing Regulations concerning devices without an intended medical purpose,
in Uncategorized
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WHO issues Global atlas of medical devices 2022,
in Uncategorized
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MDCG 2022-16 Guidance on Authorised Representatives MDR and IVDR issued,
in Uncategorized
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MDCG issues new revision of MDCG 2021-22,
in Uncategorized
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MDCG 2022-15 issued on Guidance on appropriate surveillance regarding the transitional provisions under Article 110 of the IVDR,
in Uncategorized
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MDCG 2022-14 Transition to the MDR and IVDR Notified body capacity and availability of medical devices and IVDs,
in Uncategorized
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Published: MDCG 2022-12 Guidance on harmonised administrative practices and alternative technical solutions until Eudamed is fully functional (IVDR),
in Uncategorized
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Regulation (EU) 2022/1107 issued on IVDR common specifications for certain class D devices,
in Uncategorized
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Blue Guide on Implementation of EU product rules 2022 published,
in Uncategorized
