FAQ document from Commission
The Commission published Frequently asked questions on medecines and medical devices concerning sanctions adopted following Russia’s military aggression against Ukraine and Belarus'faqs-sanctions-russia-medical_en
The Commission published Frequently asked questions on medecines and medical devices concerning sanctions adopted following Russia’s military aggression against Ukraine and Belarus'faqs-sanctions-russia-medical_en
Team-NB-PositionPaper-ConfAssessment-Multiplexassays-V1 Thanks to the work of the IVD working group, Team-NB came with a Position Paper on “Conformity assessment of multiplex assays” The paper has been approved by a large majority of members designated in the IVD sector.
The “Notice to manufacturers to ensure timely compliance with MDR requirements has been published MDCG-2022-11-PositionPaper
The draft published today in the “Notification system” of European standardisation is open for feedback until 30 June 2022 https://ec.europa.eu/growth/single-market/european-standards/notification-system_en#future
In the absence of an update of the MRA to include Regulation (EU) 2017/746, the part of the MRA chapter covering in vitro diagnostic medical devices ceases to apply as of 26 May 2022. Standardized confirmation letter rev 1 IVDDApr22(1)
Harmonised European standards in support of the Medical Devices Regulation (EU) 2017/745 (MDR) have been adopted on 17 May 2022 to be published in the Official Journal of the European Union (OJEU): https://ec.europa.eu/transparency/documents-register/detail?ref=C(2022)3003
The annual Team-NB sector press release is available via the blue Team-NB Documents button below the picture
Harmonised European standards in support of the In VitroDiagnostic Medical Devices (IVDR) have been adopted on 11 May 2022 to be published on 12 May in the Official Journal of the European Union CELEX 32022D0729 EN TXT
More info in the attached document (COM-NB)_ZB_gc_Ukraine recommandations_1909181
The association meeting is scheduled on April 6th.