The Mi-CARE Project
Children, adolescents and families with migration experiences face unique and often daunting challenges when navigating the healthcare systems in Europe. From specific healthcare needs resulting from their migration journey, to language barriers and unfamiliar healthcare processes, they are often at a disadvantage when it comes to receiving the needed care.
Research to address these challenges is essential to ensure that every child, regardless of their background, receives the best possible healthcare.
Therefore we want to learn your thoughts and experiences in the Mi-CARE project!
The Mi-CARE project enables children, adolescents, and families with migration experience, and the healthcare professionals who work with them, to identify and prioritise their most important unanswered research questions in paediatric migrant health in Europe.
We are gathering insights and experiences from people with experience in healthcare systems across Europe, as well as thoughts on what improvements are needed to enhance their care.
Our survey is completely anonymous and takes only 5 to 15 minutes to complete.
MiCare Resources
Help Us Spread the Word
Please also download and print our flyers!
It would be amazing if you could spread them in places like hospitals, community centres, asylum centres, schools, libraries, or anywhere you think it could reach families and children who may have valuable insights to share with us through our survey.
Currently, flyers are available in English, German, French, Italian, Ukrainian, Arabic, Turkish and Polish. If you need flyers in other languages, feel free to reach out to us at micare.psp@gmail.com. You can download the flyers using the link below.
About the Steering Group:
This PSP is led by the Mi – CARE Steering Group: a group of 14 healthcare professionals and people with lived experience of migration from diverse backgrounds and countries around the world. Through our research and initiatives, including this survey, we aim to improve healthcare for migrant children and adolescents across Europe.
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.