ÖversiktEU har reviderat regelverket som består av tre direktiv för att spegla utvecklingen under de senaste 20 åren.Förbered digManufacturer IVDManufacturers MDManufacturers of devices without an intended medical purposeHealthcare professionals and health institutionsThe procurement of MDs and IVDsAuthorised Representatives, Importers and DistributorsCompetent authorities in non-EU/EEA countriesVägledningEU-kommissionen tillhandahåller en rad vägledande dokument för att hjälpa de berörda aktörerna att genomföra förordningarna om medicintekniska… Latest updatesNews announcement5 augusti 2022Call for EU reference laboratories sent to Member StatesNews announcement5 juli 2022Commission Implementing Regulation (EU) 2022/1107 of 4 July 2022 laying down common specifications in accordance with Regulation (EU) 2017/746News announcement21 juni 2022Setting the scene for EU reference labs for high-risk diagnosticsNews announcement24 maj 2022Notice to Stakeholders: Status of the EU-Switzerland Mutual Recognition Agreement (MRA) for in vitro diagnostic medical devicesVisa alla HighlightsNews announcement5 augusti 2022Call for EU reference laboratories sent to Member StatesBenchmarks for high-risk diagnosticsNews announcement21 juni 2022Setting the scene for EU reference labs for high-risk diagnostics26 May 2022, the Regulation (EU) 2017/746 on In Vitro Diagnostic Medical Devices is applicable within the EUNews announcement26 maj 2021Notice to Stakeholders: Status of the EU-Switzerland Mutual Recognition Agreement (MRA) for medical devicesGeneral publications10 juli 2020State of play of Joint implementation Plan on actions considered necessary to ensure the sound functioning of the new framework for medical devices under the MDRThe UDI Helpdesk is live. It helps the economic operators in the implementation of the requirements introduced by the new UDI systemGetting ready for the new medical devices regulations – Factsheets on the main areas of the medical devices sector activities Events07maj2021Möten med samarbetspartnerWebinar for Patients – Safe and performant Medical Devices for all DocumentsEventsPublications
ÖversiktEU har reviderat regelverket som består av tre direktiv för att spegla utvecklingen under de senaste 20 åren.
Förbered digManufacturer IVDManufacturers MDManufacturers of devices without an intended medical purposeHealthcare professionals and health institutionsThe procurement of MDs and IVDsAuthorised Representatives, Importers and DistributorsCompetent authorities in non-EU/EEA countries
VägledningEU-kommissionen tillhandahåller en rad vägledande dokument för att hjälpa de berörda aktörerna att genomföra förordningarna om medicintekniska…
News announcement5 juli 2022Commission Implementing Regulation (EU) 2022/1107 of 4 July 2022 laying down common specifications in accordance with Regulation (EU) 2017/746
News announcement24 maj 2022Notice to Stakeholders: Status of the EU-Switzerland Mutual Recognition Agreement (MRA) for in vitro diagnostic medical devices
26 May 2022, the Regulation (EU) 2017/746 on In Vitro Diagnostic Medical Devices is applicable within the EU
News announcement26 maj 2021Notice to Stakeholders: Status of the EU-Switzerland Mutual Recognition Agreement (MRA) for medical devices
General publications10 juli 2020State of play of Joint implementation Plan on actions considered necessary to ensure the sound functioning of the new framework for medical devices under the MDR
The UDI Helpdesk is live. It helps the economic operators in the implementation of the requirements introduced by the new UDI system
Getting ready for the new medical devices regulations – Factsheets on the main areas of the medical devices sector activities
07maj2021Möten med samarbetspartnerWebinar for Patients – Safe and performant Medical Devices for all
