Designation of EU reference laboratories
5 laboratories designated covering the 4 categories of class D devices. More info: MDCG-2023-2713-COMMISSION-IMPLEMENTING-REGULATIONEU.pdf
5 laboratories designated covering the 4 categories of class D devices. More info: MDCG-2023-2713-COMMISSION-IMPLEMENTING-REGULATIONEU.pdf
The third session is fully booked, TEAM-NB set up a new date for the MDR technical documentation training for manufacturers on March 27th , 2024. MDR Technical Documentation Training for Manufacturers For registration, follow the link: ManufacturerTraining
Both 1st sessions are fully booked, TEAM-NB set up a new date for the IVDR technical documentation training for manufacturers on February 1st, 2024. IVDR Technical Documentation Training for Manufacturers For registration, follow the link: ManufacturerTraining
The press release is presenting the outcomes of the course and the progress of the manufacturers towards their transition to MDR thanks to responses of the attendants. Info on the 1st MDR training session : PressRelease-Training-for-MD-manufacturers-20231123
Both 1st sessions are fully booked, TEAM-NB set up a new date for the MDR technical documentation training for manufacturers on February 7th , 2024. MDR Technical Documentation Training for Manufacturers For registration, follow the link: ManufacturerTraining
This press release is a call to action to apply with notified bodies in time especially for high-risk IVD medical devices. Team-NB-PressRelease-Capacity-NotifiedBodies-during-transition-IVDR-MDR-October2023
All the Notified Bodies designated and the concerned stakeholders have been invited to different meetings taking place on October 17th to 19th. These meetings will take place remotely.
Following the November 7th session is fully booked, TEAM-NB set up a new date for the MDR technical documentation training for manufacturers on December 14th. MDR Technical Documentation Training for Manufacturers For registration, follow the link: ManufacturerTraining
The Q&A on transitional provisions for products without an intended medical purpose covered by annex XVI of the MDR is available on the Commission website on Medical Devices md_new-reg_annex-xvi_q-n-a_transition-prov
A training dedicated to help manufacturers to clarify the MDR Technical Documentation requirements is planned on November 7th. MDR Technical Documentation Training for Manufacturers For registration, follow the link: ManufacturerTraining