YleiskatsausEU on tarkistanut kolmen direktiivin oikeudellista kehystä 20 viime vuoden aikana tapahtuneen edistyksen huomioon ottamiseksi.ValmistautuminenManufacturer 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 countriesOhjeetEuroopan komissio on laatinut useita ohjeasiakirjoja, joiden on tarkoitus auttaa eri toimijoita lääkinnällisiä laitteita koskevien asetusten… Latest updatesNews announcement30 marraskuu 2022Updated information pack for candidate EU reference laboratories publishedNews announcement5 elokuu 2022Call for EU reference laboratories sent to Member StatesNews announcement5 heinäkuu 2022Commission Implementing Regulation (EU) 2022/1107 of 4 July 2022 laying down common specifications in accordance with Regulation (EU) 2017/746News announcement21 kesäkuu 2022Setting the scene for EU reference labs for high-risk diagnosticsKatso kaikki HighlightsNews announcement5 elokuu 2022Call for EU reference laboratories sent to Member StatesBenchmarks for high-risk diagnosticsNews announcement21 kesäkuu 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 toukokuu 2021Notice to Stakeholders: Status of the EU-Switzerland Mutual Recognition Agreement (MRA) for medical devicesGeneral publications10 heinäkuu 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 Events07tou2021KumppanikokouksetWebinar for Patients – Safe and performant Medical Devices for all DocumentsEventsPublications
YleiskatsausEU on tarkistanut kolmen direktiivin oikeudellista kehystä 20 viime vuoden aikana tapahtuneen edistyksen huomioon ottamiseksi.
ValmistautuminenManufacturer 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
OhjeetEuroopan komissio on laatinut useita ohjeasiakirjoja, joiden on tarkoitus auttaa eri toimijoita lääkinnällisiä laitteita koskevien asetusten…
News announcement30 marraskuu 2022Updated information pack for candidate EU reference laboratories published
News announcement5 heinäkuu 2022Commission Implementing Regulation (EU) 2022/1107 of 4 July 2022 laying down common specifications in accordance with Regulation (EU) 2017/746
26 May 2022, the Regulation (EU) 2017/746 on In Vitro Diagnostic Medical Devices is applicable within the EU
News announcement26 toukokuu 2021Notice to Stakeholders: Status of the EU-Switzerland Mutual Recognition Agreement (MRA) for medical devices
General publications10 heinäkuu 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
