Standards that matter

The United Voice of Paediatrics and Child Health

The European Academy of Paediatrics exists to promote the health of children and young people in Europe. It aims to improve standards in training, service and research and to represent the professional interests of paediatricians in the EU. It closely collaborates with the European Union of Medical Specialists and therefor has influence in the political arena to advocate for children and young people as well as for the profession.

About Us

Latest News & Updates​

More Updates...

EAP Webinar Series 2025 – Resurgence of Measles and Pertussis in Europe and Globally – The Crucial Role of Vaccination in Prevention.

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Safeguarding Childhood: EAP Meets European Union Institutions

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REACH Project: Paediatric Migrant Health in Europe

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2025 and 2026 – Important Update: EAP, CEPAS and EAP Congress and MasterCourse

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Exciting Milestone for Child Health: EAP and WHO Collaborate!

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Choosing Wisely

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UPCOMING EVENTS

EAP’S EVENTS
ALL ACROSS
EUROPE

EAP offers you many events at different times and in different European geographies. You can follow the events on our page.

Upcoming Events

EAP BOARD EXAM

18 NOVEMBER 2025

The European Board of Paediatrics – EAP online examination (EBP-EAP) has been developed in collaboration with CESMA and UEMS to assess knowledge in essential paediatric training.

Days
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Young EAP

Professional development, networking, and collaboration

Executive Committee

Guiding our organisation towards its strategic goals
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Councils

Influence paediatric care policies

Strategic Advisory Groups

Contribute with specialist focus

We need your voice

Meet EAP's Change Makers

Be Part of the Change

Engaging Community

Experience the EAP Community Up Close

It’s not just about the knowledge shared; it’s the genuine connections you will make that set our events apart. Join us and see why being part of the Global EAP family is so inspiring.

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Your Enquiries Are Welcome

We will respond to you by Email

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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:

  • BERTHOLD KOLETZKO
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