1. Winter Meeting 2024
    Saturday, 7 December 2024 Brussels
  1. Winter Meeting 2023
    Saturday, 2 December 2023 Brussels
  2. Winter Meeting 2022
    Saturday, 3 December 2022 Brussels
  3. Winter Meeting 2021
    Saturday, 4 December 2021 Virtual
  4. Winter Meeting 2020
    Sunday, 24 January 2021 Virtual
  5. Winter Meeting 2019
    Saturday, 7 December 2019 Brussels
  6. Winter Meeting 2018
    Saturday, 8 December 2018 Brussels
  7. Winter Meeting 2017
    02 December 2017 Brussels
  8. Winter Meeting 2016
    03 December 2016 Brussels
  9. Winter Meeting 2016
    30 January, 2016 Brussels

Minutes of General Assembly

Minutes of General Assembly

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Core-MD Project

Coordinating Research and Evidence for Medical Devices (CORE-MD)

New ways to test high-risk medical devices.

 

Manufacturers of medical devices need to test their products before being allowed to market them. Specifically, they require clinical data showing their medical device is safe and efficient. In this context, the EU-funded CORE-MD project will translate expert scientific and clinical evidence on study designs for evaluating high-risk medical devices into advice for EU regulators. The project will propose how new trial designs can contribute and suggest ways to aggregate real-world data from medical device registries.


It will also conduct multidisciplinary workshops to propose a hierarchy of levels of evidence from clinical investigations, as well as educational and training objectives for all stakeholders, to build expertise in regulatory science in Europe. 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, recommend how new trial designs can contribute, and advise on methods for aggregating real-world data from medical device registries with experience from clinical practice 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.

EAP Representative: