The 14th Annual International Congress of Arthroplasty Registries was held from 19 to 21 february 2025 in Christchurch (Nuova Zelanda). For further information please visit ISAR website. Available in the “Attachments” for consultation and download the abstract presented by Riap Research Group.
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 third Webinar entitled “Training and education for regulators, for notified bodies and clinicians” was held on Zoom on July 10, 2023, from 17.00 to 18.15 (attached, the program of the …
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 third Webinar entitled “Objective performance criteria for medical devices” was held on Zoom on April 3, 2023, from 17.00 to 18.15 (attached, the program of the event). Registration link. To …
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 second Webinar entitled “The origins and objectives of European regulations for medical devices” was held on Zoom on March 6, 2023, from 17.00 to 18.15 (attached, the program of the …
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 first Webinar entitled “Orthopaedic implants and European Medical Device Regulations” was held on Zoom on January 30, 2023, from 17.00 to 18.15 (attached, the program of the event). To be …
11th Annual International Congress of Arthroplasty Registries
Dublin – September 3-5, 2022
The video describing the RIAP through a series of questions and answers is now available online. Together with Eng. Marina Torre (RIAP and RIPI Project Leader) we learn about the reasons that made RIAP a real forerunner in monitoring implantable devices, as well as its history, structure and future outlook. In 2006, the implementation of …
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 now comply with the MDR. After the transitional period and a delay due to the COVID-19 emergency, this is an important date for manufacturers and their authorized representatives, as well …