Protecting Children from Alcohol-Related Harm: EAP Takes the Conversation to the World Health Summit

October 11, 2026

Alcohol Does Not Have to Be in a Child’s Glass to Cause Harm

At the World Health Summit 2026 in Berlin, EAP and EHAA hosted a dedicated side meeting, in collaboration with WHO/Europe, ESPGHAN, EFAD, EAN and ESR, to put children’s health and rights at the centre of alcohol policy.

On 11 October 2026, the European Academy of Paediatrics (EAP) and the European Health Alliance on Alcohol (EHAA) are hosting a dedicated side meeting at the World Health Summit in Berlin, bringing together leading European health organisations to address this challenge.

No single specialty sees the whole picture

Alcohol-related harm in children is about much more than underage drinking. It can begin before birth, affect children growing up in families where alcohol misuse is present, and continue into adolescence, when the developing brain is particularly vulnerable. Yet children are not always at the centre of discussions about alcohol policy and prevention.

For paediatricians, the consequences of alcohol exposure can appear in many different forms:

 

  • Before birth: Prenatal alcohol exposure can have lifelong neurodevelopmental and other health consequences, including Fetal Alcohol Spectrum Disorder (FASD).

  • During childhood: Parental alcohol misuse can contribute to adverse childhood experiences, neglect, violence and disrupted family environments.

  • During adolescence: Alcohol use can affect the developing brain and contribute to neurological, cognitive and mental-health risks.

  • Across multiple systems: Alcohol-related harm can involve neurological, gastrointestinal, hepatic, nutritional, metabolic and developmental health.

These consequences often cross the boundaries of individual specialties. Recognising, preventing and addressing them requires a coordinated approach.

About the Meeting

Six organisations came together at the World Health Summit side event roundtable to highlight the scale and consequences of alcohol-induced harm and the urgent need for stronger prevention policies.

With a full room and lively, in-depth discussions, the event brought together different perspectives and expertise around a shared commitment to advancing public health.

We are excited to leave the discussion with a concrete next step. The establishment of a joint working group, coordinated under the umbrella of the European Academy of Paediatrics (EAP) in collaboration with EHAAh, will help turn this momentum into action.

The EAP is proud to provide a platform for this collaboration and looks forward to working with its partners to move these priorities forward.

“Many public health problems are described as alcohol-related when they are, in fact, alcohol-induced. Alcohol is often the catalyst behind preventable harm, and recognising its role is essential to effective prevention. 

We already have the expertise and the right people around the table. Now we need to keep this collaboration going, secure EU funding and translate our shared knowledge into action. From prenatal alcohol screening and early identification of fetal alcohol spectrum disorders to adolescent prevention and stronger alcohol policies, we need coordinated efforts, evidence-based national guidelines and a stronger commitment to prevention across Europe.”

The EAP is proud to provide a platform for this collaboration and looks forward to working with its partners to move these priorities forward.

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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: