New medical device regulations: the regulator’s view
Melvin T, Torre M. New medical device regulations: the regulator’s view. Efort Open Reviews 2019; 4: S140-S145.
Melvin T, Torre M. New medical device regulations: the regulator’s view. Efort Open Reviews 2019; 4: S140-S145.
What is Riap? What are the goals? What information is collected? How is Riap organized? Why a registry, and why a national registry? How is the implanted device identified? How personal data are treated (Privacy)?
International Orthopaedics (SICOT) (2018)
In: 7th International Congress of Arthroplasty Registries. June 9-11, 2018, Reykjavik, Iceland
In: 7th International Congress of Arthroplasty Registries. June 9-11, 2018, Reykjavik, Iceland
Addendum to: “Italian Arthroplasty Registry Project. Better data quality for better patient safety. Fourth Report 2017”
English version of Tables and Figures. Rome: Il Pensiero Scientifico Editore, 2018
Cross-cultural adaptation and validation of the Italian version of the Hip disability and Osteoarthritis Outcome Score (HOOS) M. Torre, I. Luzi, F. Mirabella, M. Del Manso, G. Zanoli, G. Tucci, E. Romanini Health and Quality of Life Outcomes (2018) 16:115
International Strategic workshop Tools to identify and characterize implantable devices: the perspective of the RIAP-NJR collaboration 1st march 2018.
Monitoring Outcome of Joint Arthroplasty in Italy: Implementation of the National Registry