On Friday 17 February 2023, as part of the II level Master’s Degree in “Clinical Governance of medical and diagnostic devices”, organized by Cattolica University, …
Within the European project CORE-MD (Coordinating Research and Evidence for Medical Devices), in which the Italian National Institute of Health participates as a partner, the …
Bacocco DL, Carrani E, Ciciani B, Di Sanzo P, Leotta F, Torre M. Design and implementation of the new Italian healthcare digital interoperable registry for …
Toccaceli V, Torre M. A far-reaching Regulation for the Italian National Registry of Implantable Prostheses: a possible model for other health registries. Ann Ist Super …
Zecchin M, Torre M, Carrani E, Sampaolo L, Ciminello E, Ortis B, Ricci R, Proclemer A, Sinagra G, Boriani G. Seventeen-year trend (2001–2017) in pacemaker …
Torre M, Carrani E, Franzò M, Ciminello E, Urakcheeva I, Bacocco DL, Valentini R, Pascucci S, Madi S, Ferrara C, Toccaceli V, Sampaolo L, Ceccarelli …
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 …
