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Regulation (EU) 2017/746 on in vitro diagnostic medical devices (the IVDR) requires that the manufacturer shall draw up a summary of safety and performance (SSP) for class C and D devices, other than devices for performance studies. The SSP shall be validated by a notified body (NB) and made available to the public via the European database on medical devices (Eudamed). Text elements in italic i..

The European Commission (EC) has made a proposal (COM(2024)43/ 5712/24) to delay compliance of legacy IVD devices and for EUDAMED to be rolled out by modules completed. The proposal would extend the time for manufacturers of legacy IVDs to become compliant with the IVDR. Also, analogous to Regulation (EU) 2023/607, requires an application with a notified body designated for the IVDR and an agree..

In 2017, the EU introduced new rules for medical devices and in vitro diagnostics to ensure a better protection of public health and patient safety. Despite considerable progress in transitioning to these rules and the additional time given to the sector to implement them, the transition remains slow. In 2023, the Commission took measures to ensure the availability of medical devices. Today, we ..

유럽연합과 스위스와의 협정 (MRA, Mutual Recognition of Conformity Assessments)이 만료가 됨 스위스는 유럽연합에서 제3국으로 처리 됨 ('third country') 스위스 자체 의료기기 DB 구축 (유럽연합의 EUDAMED와 유사) 현재는 강제사항 아님 (2023년 08월 기준) DB: swissdamed 예상일정 swissdamed – Swiss Database on Medical Devices (swissmedic.ch) swissdamed – Swiss Database on Medical Devices In April 2022, Swissmedic started design work on the “swissdamed” database. Please note ..