Medical device regulatory science
3 European H2020 organizations list this as part of their work.
Most active in this area
- SOCIETE EUROPEENNE DE CARDIOLOGIE
Europe's largest cardiology society, contributing clinical registries, guideline expertise, and pan-European physician networks to cardiovascular research consortia.
“Coordinated CORE-MD, focused on evidence standards and trial methodologies for high-risk medical devices — a departure from pure clinical research.”
FR15 projects - UMIT TIROL - PRIVATE UNIVERSITAT FUR GESUNDHEITSWISSENSCHAFTEN UND TECHNOLOGIE GMBH
Austrian private health sciences university contributing epidemiology, biomonitoring, medical device regulation, and nature-based health intervention expertise to EU consortia.
“Participated in CORE-MD, focused on evidence-based evaluation of high-risk medical devices, trial methodologies, and device registries under the new Medical Device Regulation.”
AT5 projects - INSEL GRUPPE AG
Swiss university hospital group contributing clinical trial sites, cardiovascular expertise, and medical device validation to European health research consortia.
“CORE-MD addresses evidence standards for high-risk medical devices in cardiology, orthopaedics, and diabetes.”
CH4 projects