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Clinical Investigation Plans The Role Of MDCG 2024-3 In The Context Of EU MDR Annex XV ISO 14155

In vitro diagnostics and the European Database on Medical Devices (EUDAMED) - guide — EUbusiness com

The European Commission proposed on 23 January more time for companies to apply the In Vitro Diagnostic Medical Devices Regulation (IVDR), under certain conditions, as well as measures to enhance transparency in the medical device sector including speeding up the launch of some elements of the European Database on Medical Devices - EUDAMED.

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