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Funded Projects › H2020

CORE-MD · Coordinating Research and Evidence for Medical Devices

H2020Status: CLOSED1 April 202131 March 2024EU funding €2,360,978Call H2020-SC1-BHC-2018-2020

CORE–MD will translate expert scientific and clinical evidence on study designs for evaluating high-risk medical devices into advice for EU regulators, to achieve an appropriate balance between innovation, safety, and effectiveness. A unique collaboration between medical associations, regulatory agencies, notified bodies, academic institutions, patients’ groups, and health technology assessment agencies, will systematically review methodologies for the clinical investigation of high-risk medical devices (Work Package 1), recommend how new trial designs can contribute (Work Package 2), and advise on methods for aggregating real-world data from medical device registries with experience from clinical practice (Work Package 3). Multidisciplinary workshops will propose a hierarchy of levels of evidence from clinical investigations; educational and training objectives for all stakeholders, to build expertise in regulatory science in Europe; and an ethics charter for medical device innovation (Work Package 4). Industry participation will be invited. Specific CORE–MD tasks will advise on optimal statistical methods, the utility of patient-reported outcomes, the conduct of registry trials, clinical criteria for evaluating artificial intelligence as a medical device, and how to evaluate medical devices used in children. The essential principles of medical device trials will be considered jointly with the Good Clinical Trials Collaborative. Links between CORE–MD partners will catalyse sustainable networks for research. The consortium is led by the European Society of Cardiology and the European Federation of National Associations of Orthopaedics and Traumatology, and involves all 33 specialist medical associations that are members of the Biomedical Alliance in Europe. Final recommendations will be submitted to the Working Group on Clinical Investigation and Evaluation of the European Commission to be considered when developing EU guidance or common specifications.

Consortium · 23 organisations

coordinator

SOCIETE EUROPEENNE DE CARDIOLOGIE

FR · €448,140

participant

ACADEMISCH ZIEKENHUIS LEIDEN

NL · €367,895

participant

BIOMEDICAL ALLIANCE IN EUROPE

BE · €52,024

participant

FORUM DES PATIENTS EUROPEENS

BE · €57,650

participant

EUROPEAN ACADEMY OF PAEDIATRICS

BE · €58,563

participant

HTA AUSTRIA - AUSTRIAN INSTITUTE FOR HEALTH TECHNOLOGY ASSESSMENT GMBH

AT · €52,969

thirdParty

UNIVERSIDAD DE GRANADA

ES

participant

ISTITUTO SUPERIORE DI SANITA

IT · €64,428

participant

LAEGEMIDDELSTYRELSEN

DK · €21,250

participant

INSEL GRUPPE AG

CH · €106,400

participant

EFORT

CH · €199,169

participant

HEALTH PRODUCTS REGULATORY AUTHORITY

IE · €50,000

participant

THE EUROPEAN ASSOCIATION MEDICAL DEVICES-NOTIFIED BODIES

BE · €39,000

participant

URZAD REJESTRACJI PRODUKTOW LECZNICZYCH, WYROBOW MEDYCZNYCH I PRODUKTOW BIOBOJCZYCH

PL · €10,000

participant

RIJKSINSTITUUT VOOR VOLKSGEZONDHEID EN MILIEU

NL · €86,605

participant

POLITECNICO DI MILANO

IT · €108,750

participant

REGION UPPSALA

SE · €92,220

participant

THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD

UK · €135,566

participant

KATHOLIEKE UNIVERSITEIT LEUVEN

BE · €100,026

participant

FUNDACION PUBLICA ANDALUZA PROGRESO Y SALUD M.P.

ES · €48,775

participant

GOETEBORGS UNIVERSITET

SE · €48,249

participant

UMIT TIROL - PRIVATE UNIVERSITAT FUR GESUNDHEITSWISSENSCHAFTEN UND TECHNOLOGIE GMBH

AT · €103,400

participant

ROYAL COLLEGE OF SURGEONS IN IRELAND

IE · €109,900

Research fields

View the official record on CORDIS →

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Source: CORDIS, Publications Office of the European Union. Global Research Partnerships surfaces open EU research data to help you find collaborators; we are not affiliated with the European Union.