On the 26th of May 2021, the new Medical Devices Regulation (EU) 2017/745 (MDR) came into effect. Medical devices placed on the EU market must …

CORE-MD, the first European project to identify ways to enable the scientific, fair, and systematic evaluation of medical devices, has been officially launched on 16 …

The report “Impact of COVID-19 pandemic emergency on joint arthroplasties in seven Italian Regions. Version of March 17, 2021” (Rapporto ISS COVID-19 n. 7/2021*) is …

To allow national authorities, notified bodies, manufacturers and other key actors to fully focus on coronavirus-related priorities, the European Council and Parliament adopted Regulation 2020/561 …