Opening Words
Opening Conversation: Health is Power
In a period marked by geopolitical uncertainty, technological transformation and mounting pressure on Europe’s economic and social models, health is becoming increasingly central to the continent’s resilience,competitiveness and strategic stability. No longer confined to healthcare policy alone, health now sits at the intersection of economic security, industrial capacity, innovation, preparedness and societal cohesion. As Europe redefines its priorities for the years ahead, the conversation is increasingly shifting from how to manage healthcare systems to how health can strengthen Europe’s long-term prosperity, resilience and global position in a rapidly changing world. In this context, an equally important question is whether European and national governance models are adapting fast enough to reflect health’s growing role across economic, industrial and security agendas
Biotech Made in Europe: What Would It Take to Foster Global Champions
Europe has built a strong foundation in scientific excellence and biotechnology innovation, yet translating this strength into sustainable investment, industrial capacity and patient impact remains a defining challenge. As the next generation of biotech advances, Europe must ensure that health systems are equipped to absorb transformative innovations, recognising health innovation not only as a cost but as an investment in long-term health-system capacity, productivity and resilience. At the same time, creating the conditions for biotech companies to invest, conduct research, manufacture and scale within Europe will be critical to strengthening the continent’s strategic position. The extent to which Europe can turn scientific leadership into lasting value will depend on its ability to align innovation, patient access and investment conditions across the biotechnology ecosystem, ensuring that Europe remains a place where breakthrough ideas can be developed and delivered.
Coffee Break
Health is Not a Cost: Building Europe’s Strategic Health Economy
For decades, health expenditure has largely been framed as a fiscal burden rather than a driver of economic resilience and growth. Yet in ageing societies facing workforce shortages, productivity pressures and rising geopolitical competition, health increasingly functions as strategic economic infrastructure. Resilient health systems, healthy populations and innovation capacity are central to long-term prosperity, stability and sovereignty, and a high-priority position for health within Europe's competitiveness, industrial, resilience and economic agenda can no longer be neglected. Treating health as a cost to be contained, rather than a capacity to be built, risks leaving Europe less able to compete, less able to innovate, and less able to stand on its own.
Beyond Frameworks, Towards Resilience: EU’s Pharmaceutical Future and Industrial Base
The European healthcare landscape is set to be redefined for the decades to come by the implementation of the General Pharmaceutical Legislation (GPL) and the Critical Medicines Act (CMA), alongside emerging frameworks such as the Biotech Act and the Public Procurement Act. As Europe navigates an increasingly complex geopolitical environment, these regulatory files share the vital goals of accelerating patient access, securing supply chain resilience and strengthening industrial competitiveness, but their ultimate success hinges on creating an integrated and coherent framework. The extent to which this evolving framework can support sustainable progress will depend in part on its ability to incentivize investment across the entire value chain: from early-stage R&D and intermediate manufacturing phases to timely market access. A greater strategic and coordinated approach will be essential to safeguarding Europe’s capacity to innovate and manufacture, reinforcing pharmaceuticals as a strategic industrial pillar, and delivering sustainable health solutions across the continent
High-Level VIP lunch
Networking Lunch
Financing the Next Chapter: Can Europe Secure Future Biomedical Breakthroughs?
Europe is entering a new chapter in its approach to biotech and life sciences competitiveness. Over the past two decades, its share of innovative medicines has declined, while the US has consolidated its leadership and China has rapidly gained ground. At the same time, Europe continues to generate world-class science but too often struggles to finance, scale and deploy innovation at the same pace as its global competitors, putting at risk not only medicines, but also clinical research, high-value jobs, scientific talent and the wider innovation ecosystem linking universities, hospitals, companies and patients. From the Biotech Act and Capital Markets Union discussions to renewed focus on strategic technologies and industrial resilience, the window is open for real action by mobilising long-term capital, improving the conditions for biotech investment and scaling, and ensuring that Europe’s scientific excellence can translate into lasting economic and strategic leadership.
Winning Back Clinical Research: Data Governance and the Biotech Act
Health data is becoming one of the defining strategic assets of the global innovation race. As biomedical discovery, diagnostics and personalised medicine advance, the way Europe governs and mobilises health data within clinical research will directly shape its competitiveness, innovation capacity and technological sovereignty. The Biotech Act, currently under negotiation, is positioned as the great promise to reshape how health data is processed within clinical trials. By proposing a single, harmonised legal basis for processing clinical trial data, and by enabling data collected in one trial to be reused for further research, the Biotech Act addresses one of the most persistent bottlenecks in European clinical research: years of fragmentation, legal uncertainty and delay caused by divergent national approaches to data protection.Europe's attractiveness for clinical trials and the revival of its research engine will depend on the Biotech Act's real-world delivery and the balance it manages to strike.
Closing Remarks
Opening Remarks
Open, Resilient, Competitive: Europe’s Oncology Advantage
As oncology research and innovation become increasingly complex and promising, Europe must ensure its scientific leadership translates into value and impact. While the European value concept is shaping EU policy, there is a growing focus on strengthening Europe’s capacity to develop, scale and manufacture health innovation while reducing dependencies. For oncology, this emphasis raises broader questions: how can Europe strengthen its strategic capacity while preserving the openness and collaboration needed to bring innovative therapies to patients? What does this mean in practice for Europe’s ability to attract investment and retain the talent needed to develop clinical trials and build manufacturing capacity? How can European preference support strategic capabilities without limiting competition or access to global expertise, technologies and supply chains? And how can Europe ensure that the value created by its ecosystem ultimately translates into better and more timely access for European patients?
From Lab to Life: Full-Lifecycle Innovation for Under-Recognised Chronic Diseases
While Europe’s life sciences ecosystem continues to drive breakthroughs in areas like oncology and advanced therapies, millions of patients living with severe, high-burden chronic conditions remain underserved. The challenge spans across the full lifecycle of innovation: from weak incentives for research and development, to health systems not recognizing the true societal and psychological burden of these diseases – making them, in turn, difficult to be considered as priorities for investment. Immune-mediated skin diseases – such as psoriasis, vitiligo, and atopic dermatitis – are a clear illustration of this systemic gap. Frequently dismissed by health systems as merely "cosmetic," these conditions carry a profound, chronic, life-altering burden that is rarely captured in traditional health frameworks. These conditions often begin in adolescence and early adulthood, and persist across a patient's entire life, with a huge cost to society: lost education, reduced workforce participation, and diminished productivity over decades.
High-Level VIP lunch
Networking Lunch
From Vaccine Uptake to Economic Resilience: The Case for Life-Course Immunisation
Life-course immunisation should be understood not only as a public health measure, but as an investment in Europe’s economic resilience. In a context of rising healthcare costs, workforce shortages and growing pressure on health systems, where an ageing society plays a huge role, prevention offers a clear cost-benefit logic: avoiding disease is often less costly than treating its consequences. At the same time, declining vaccine trust and falling uptake rates are creating and bringing back risks. In a more mobile and interconnected world, infectious diseases are not contained by borders, and the re-emergence of vaccine-preventable diseases shows that prevention cannot be taken for granted. Strengthening life-course immunisation should therefore be a priority: not only to protect individual health, but to safeguard health system sustainability, economic productivity and public resilience, and to adapt health systems to the demographic change.
CE Marked, but for Whom? Beyond Approval, Towards Adoption
The ambition is clear: to reshape Europe’s medical technologies ecosystem and foster innovation. Through the proposed MDR/IVDR amendments and the Digital Omnibus on AI, the direction is increasingly explicit: a more competitive, innovation-friendly and predictable framework for health technologies. But the CE mark is not everything. A device may be safe, compliant and legally available, yet still fail to reach patients if hospitals cannot buy it, integrate it or sustain its use. In medical technologies, value often depends not only on the product, but on training, infrastructure, interoperability, service models, workflow adaptation and long-term outcomes. This creates a sharper challenge across Europe: innovation may be adopted quickly in well-resourced Member States, regions and hospitals, while others remain unable to absorb it. If procurement rewards the lowest upfront price, if implementation capacity varies widely, and if value is defined differently across territories, certified innovation can end up reinforcing existing inequalities. The vision now moves forward regulating innovation, to whether Member States and regions can recognise and adopt it.
Health, Preparedness and Europe’s Security Agenda
Health security is increasingly becoming part of Europe’s broader resilience and security agenda. From biosecurity threats and critical supply chains to civil-military coordination, cybersecurity and strategic stockpiling, the boundary between health policy and security policy is becoming increasingly blurred. Russia’s invasion of Ukraine, growing geopolitical fragmentation and rising concerns around biological threats have reinforced the understanding that health systems are not only social infrastructure, but also strategic assets essential to Europe’s stability and preparedness. At stake is whether Europe can build the coordination, industrial capacity and strategic foresight needed to respond not only to future pandemics, but also to a more volatile geopolitical environment where resilience, rapid response and the protection of critical health infrastructure are becoming central to European security itself.
Coffee Break
AI-Driven Innovation for Paediatric and Rare Diseases: The ERAMET Experience
Health at the Edge of Enlargement
With accession negotiations open with Ukraine, Moldova, Montenegro and Albania, among others, and broader political questions continuing around the EU’s relationship with countries such as Türkiye and Iceland, the European Health Union is at a crucial moment. As an enlarged Union will also mean an enlarged health space, questions raise for Europe’s capacity to prevent, detect and respond to cross-border health threats, from infectious diseases and antimicrobial resistance to food safety risks and future crises. It also brings a single market dimension, as future members will need to align with EU standards on medicines, medical devices, digital health, data governance, consumer protection or public procurement. At the same time, differences in investment, infrastructure, access to care and system capacity are a key piece for European equity standards, while health workforce mobility may deepen them: a wider area for freedom of movement could exacerbate the workforce shortages already present in some regions and countries.
Closing Remarks
Cocktail Reception