List of international meetings related to arthroplasty
10th International RSA Congress
13-14 May 2027 | Rimini – Italy
16th ISAR Annual International Congress of Arthroplasty Registries
22-24 May 2027
Stratford-upon-Avon – United Kingdom
NORE Events
IPSI Inaguration workshop | Brussels, Belgium, 21 January 2020
- Historical Pitfalls
by Prof. Per Kjaersgaard-Andersen | PDF | 27 pages | 2.7Mb - Safety Challenges in Arthroplasty: Surgeon’s Views
by Prof. Li Felländer-Tsai | PDF | 30 pages | 3.1Mb - Safety Challenges in Arthroplasty: Patient’s Views
by Mr. Dieter Wiek | PDF | 15 pages | 0.5Mb - Safety Challenges in Arthroplasty: Manufacturer’s Views
by Mrs. Katharina von Strünsee | PDF | 14 pages | 0.7Mb - Need for Innovation
by Prof. Francesco Benazzo | PDF | 31 pages | 6.6Mb - Surveillance and Vigilance
by Dr. Matthias Fink & Dr. Bassil Akra | PDF | 11 pages | 1Mb - The Role of Clinicians under the new MDR
by Mr. Paul Piscoi | PDF | 27 pages | 1.1Mb - Surveillance and Vigilance: Manufacturer’s Contribution
by Mr. Hassan Achakri | PDF | 9 pages | 0.3Mb - Surveillance and Vigilance: Surgeon’s Contribution
by Prof. Rob Nelissen | PDF | 31 pages | 5.6Mb - Failure Analysis – Practice and Future Challenges
by Prof. Michael Morlock | PDF | 13 pages | 2Mb
NIMAC Symposium | Brussels, Belgium, 06 April 2018
- NIMAC Symposium Programme
PDF document, 4 pages, 189kb - Welcome and Introduction
PDF document, 15 pages, 873kb - Where we stand in EFORT
PDF document, 9 pages, 451kb - The Life of a TJR The stages of regulating and monitoring a total joint replacement: Now and the future
PDF document, 26 pages, 235kb - Medical Device Regulation & Registries
PDF document, 26 pages, 586kb - Impact on Industry of the New Medical Device Regulation (MDR)
PDF document, 8 pages, 429kb - Certification of JRIs under the MDR
PDF document, 24 pages, 261kb - Scientific Evidence and Innovation in the EU
PDF document, 38 pages, 4.5Mb - Shifting paradigms for high-risk devices: lessons learned from the past
PDF document, 10 pages, 857kb - Engaging with the new EU Regulatory Landscape for medical devices – Clinical Evidence for Medical Devices
PDF document, 13 pages, 1.6Mb - Minimum Requirements, Clinical practice and Lessons learnt from the past
PDF document, 49 pages, 3Mb - Monitoring by registries or do we still need clinical trials? The Pros and Cons
PDF document, 38 pages, 5.6Mb - Postmarket surveillance & (Quality) Registries
PDF document, 24 pages, 2.2Mb - Engaging with the new EU regulatory landscape for medical device – Challenges and opportunities
PDF document, 17 pages, 580kb - The new EU MDR – lessons learned from the past
PDF document, 6 pages, 411kb