European Parliament

How to watch the Committee on Public Health (SANT)

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Latest updates

What is said in the sittings, update by update, the latest first. Each update opens the video at the second it was said.

  1. GMT+2

    Committee on Public Health Ordinary meeting

    Chair’s wrap-up on pediatric cancer and launch of TechBio session

    The Chair summarizes remaining gaps in pediatric cancer policy and funding, then formally closes that agenda item and opens a new ‘Excellence in Health Science’ exchange on TechBio and AI in drug discovery, introducing the next speaker and format.

    In this chapter

    1. Chair’s conclusions on pediatric cancer: need for money and systemsAdam Jarubas
    2. Introduction of ‘TechBio: AI-enabled future of drug discovery’Adam Jarubas

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  2. GMT+2

    Committee on Public Health Ordinary meeting

    Expert panel: regulatory incentives and access reforms

    Scientific and NGO experts outline failures of current orphan and pharma frameworks, argue for specific SPC extensions and new EU‑level funding and procurement tools, and debate with MEPs on rare disease law, EMA and HTA procedures, reimbursement delays and the design of a non‑profit academia–industry vehicle.

    In this chapter

    1. Prof. Vassal: medulloblastoma case and Biotech Act SPC incentiveAdam Jarubas
    2. Delphine Heenen: cross-border trials, public funding and joint procurementDelphine Heenen
    3. Second-panel Q&A: SPC debates, rare disease law, EMA and reimbursementAdam Jarubas

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  3. GMT+2

    Committee on Public Health Ordinary meeting

    MEP reactions and questions on EU pediatric pathway

    MEPs react to the testimonies by calling for an EU pediatric cancer pathway, stronger funding and health competences, and raise detailed questions on data, pharma obligations and existing EU instruments before the Chair closes the first segment and moves to the expert panel.

    In this chapter

    1. First MEP reactions: call for EU pathway and MFF fundingAdam Jarubas
    2. Further MEPs: prevention, rare diseases, and EU health roleIgnazio Roberto Marino
    3. Data, pharma obligations and tangible results: questions to expertsPeter Liese
    4. Guests’ closing remarks and transition to expert panelAdam Jarubas

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  4. GMT+2

    Committee on Public Health Ordinary meeting

    Opening and testimonies on childhood cancer

    The Chair opens the SANT meeting on childhood cancer, President Metsola provides the political framing and EU commitments, and survivor and parent‑economist testimonies expose treatment inequalities, market failures and the case for an EU‑level pediatric oncology pathway.

    In this chapter

    1. Opening of SANT meeting: focus on childhood cancerAdam Jarubas
    2. President Metsola: political framing and EU commitmentsRoberta Metsola
    3. Child survivor Leonor: treatment inequities and moral challengeAdam Jarubas
    4. Economist-parent Dams: biology, ultra-rare markets and need for EU pathwaySam Daems

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  5. GMT+2

    Committee on Public Health Ordinary meeting

    Commission Q&A and procedural follow-up on cross-border healthcare revision

    Members question the Commission on legal bases, information tools and sustainable EU funding as the Commission explains the interaction between the directive and social security coordination, limits on prior authorisation, digital simplification and ERN support, before the rapporteur issues a political funding call and the Chair sets amendment deadlines and closes the sitting.

    In this chapter

    1. Q&A and Commission: legal frameworks, information tools and implementationAndrás Tivadar Kulja
    2. Georgiou and Chair: political call and procedural follow-upAdam Jarubas

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  6. GMT+2

    Committee on Public Health Ordinary meeting

    Modernised cross-border healthcare rules: draft report and group positions

    Rapporteur Georgiou presents draft report priorities on updating the directive, tackling prohibitive out-of-pocket costs and securing higher EU funding, while political groups set out their positions on access, ERNs, digital health alignment, equity and patient protection against unsafe treatments abroad.

    In this chapter

    1. Rapporteur Georgiou: draft report priorities and funding demandsAdam Jarubas
    2. Political groups: positions on access, ERNs and equityLiesbet Sommen

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  7. GMT+2

    Committee on Public Health Ordinary meeting

    Legal shortcomings, ERNs and EU-level solidarity mechanisms

    Political and expert debate on whether obstacles stem mainly from national implementation or the directive itself, treatment of upfront payments and prior authorisation, potential upgrading of the directive and strengthening of ERNs, and options for new EU-level funding or solidarity instruments linked to biotech and pharmaceutical contributions.

    In this chapter

    1. Legal framework, ERNs and EU-level funding optionsTomislav Sokol
    2. MEPs and experts: barriers, authorisation and solidarity optionsPeter Agius

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  8. GMT+2

    Committee on Public Health Ordinary meeting

    EPRS assessment on cross-border healthcare: roadmap and initial reactions

    Presentation of the European Added Value Assessment on cross-border healthcare, detailing the three‑pillar roadmap on patient access, ERNs, telemedicine and the European Health Data Space, followed by rapporteur and shadow rapporteur reactions on persistent barriers, legislative versus implementation gaps, and needs of vulnerable patient groups.

    In this chapter

    1. Cross-border healthcare assessment: presentation of roadmapAdam Jarubas
    2. Rapporteur and shadows: gaps in cross-border healthcareAdam Jarubas

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  9. GMT+2

    Committee on Public Health Ordinary meeting Joint meeting Committee on the Environment, Climate and Food Safety

    Fine particles: MEP Q&A, policy implications and closing

    MEPs question the experts on mortality, inequalities, sector priorities, agriculture and regulatory ambition; experts reply on integrating health authorities, strengthening agricultural and heating rules, and targeting vulnerable groups, before final remarks on farming efforts and formal closure of the session.

    In this chapter

    1. First Q&A: mortality burden, social inequalities and policy coherenceAdam Jarubas
    2. Second Q&A: new risk factors, agriculture and regulatory ambitionAurelijus Veryga
    3. Experts’ replies on agriculture, health integration and equityAdam Jarubas
    4. Final remarks on agricultural efforts and closing of sessionAdam Jarubas

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  10. GMT+2

    Committee on Public Health Ordinary meeting Joint meeting Committee on the Environment, Climate and Food Safety

    Fine particles study: introduction and key findings

    Chairs introduce the Policy Department study on PM2.5 as a public health priority, and invited experts present scientific evidence on health impacts, trends, regulatory drivers, major remaining emission gaps and recommended upgrades to EU air‑quality and sectoral policies.

    In this chapter

    1. Introduction to study on health effects of fine particlesAdam Jarubas
    2. Study presentation: evidence on PM2.5 health impacts and policy gaps

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  11. GMT+2

    Committee on Public Health Ordinary meeting Joint meeting Committee on the Environment, Climate and Food Safety

    Biotech file: organ processing safeguards and GMMs

    Co‑rapporteurs and shadows present and debate amendments on organ processing and genetically modified microorganisms, contrasting innovation goals with strong safeguards on ethics, non‑commercial organ use, risk‑based authorisation, data protection, delegated powers and traceability, followed by Commission defence of the proposals and procedural next steps.

    In this chapter

    1. SANT rapporteur: organ processing framework and safeguardsAdam Jarubas
    2. ENVI rapporteur: GMMs: innovation with precautionMarta Temido
    3. Shadows (EPP, S&D, PfE, ECR): organ processing and GMMsAnja Hazekamp

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  12. GMT+2

    Committee on Public Health Ordinary meeting Joint meeting Committee on the Environment, Climate and Food Safety

    Opening of joint SANT–ENVI sitting and biotech agenda

    Chairs open the joint SANT–ENVI meeting, resolve technical and procedural issues, adopt the agenda and minutes, and outline the joint procedure for handling the biotech directives within the European Biotech Act framework.

    In this chapter

    1. Opening of joint SANT–ENVI meeting and agendaAdam Jarubas
    2. Procedure for biotech directives fileAdam Jarubas

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  13. GMT+2

    Committee on Public Health Ordinary meeting

    MEPs–EMA Q&A on medicines policy and regulation

    Combined Q&A rounds where MEPs question EMA on the Critical Medicines Act, shortages tools, transparency and pricing context, environmental and wastewater rules, support for ATMPs and academic developers, and the Agency’s evolving MDR/IVDR mandate, with Cooke detailing current instruments, legal limits and planned pilots. This segment concentrates the main political, regulatory and implementation issues around medicine availability, innovation pathways and the EMA’s future responsibilities.

    In this chapter

    1. Second Q&A round: Critical Medicines Act, shortages and transparencyRomana Jerković
    2. Final Q&A: contraception, environmental rules, ATMPs and MDR tasksRomana Jerković

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  14. GMT+2

    Committee on Public Health Ordinary meeting

    MDR/IVDR revision wrap‑up and agenda shift to EMA

    Closing exchanges on MDR/IVDR safety, inspections and the Commission’s risk‑based approach lead into the formal conclusion of this legislative item and the Chair’s opening of the next agenda point on EMA’s 2023 annual report, including clarification of speaking order and amendment deadlines.

    In this chapter

    1. Safety, inspections and Commission’s risk‑based approachPeter Liese
    2. Transition from MDR/IVDR file to EMA annual reportRomana Jerković

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  15. GMT+2

    Committee on Public Health Ordinary meeting

    MDR/IVDR revision: mandate, groups and opinions

    The chair and rapporteur introduce the MDR/IVDR revision mandate and six‑pillar reform approach, followed by political group reactions on safety, innovation, AI and industrial policy, and the presentation of IMCO and BUDG opinions on AI scope, oversight, financing and resources, before individual MEPs highlight practical concerns on implementation and alignment with related EU rules.

    In this chapter

    1. Chair and rapporteur: framing MDR/IVDR revisionRomana Jerković
    2. Political groups: safety, innovation, AI and industrial balanceTiemo Wölken
    3. IMCO and BUDG opinions: AI scope, oversight and financingMaria Guzenina
    4. MEPs’ catch‑the‑eye interventions on MDR revisionRomana Jerković

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  16. GMT+2

    Committee on Public Health Ordinary meeting

    2027 EU health budget: rapporteur, groups and funding choices

    The rapporteur outlines priorities for the 2027 EU health budget opinion, followed by political group reactions opposing EU4Health cuts and a broader debate on overall funding levels, spending efficiency and the amendment timetable.

    In this chapter

    1. 2027 EU health budget opinion: rapporteur prioritiesAdam Jarubas
    2. Political groups: opposition to EU4Health budget cutsVictor Negrescu
    3. EU4Health 2027 budget opinion: funding levels and closureGerald Hauser

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  17. GMT+2

    Committee on Public Health Ordinary meeting

    MEP scrutiny: data, innovation and inequalities; Minister’s replies

    A second round of MEPs links competitiveness and climate costs to health financing, raises digital health, AI, clinical trials, gender bias and the cancer ‘right to be forgotten’, followed by the Minister detailing Ireland’s stance on the EHDS, innovation, pricing, manufacturing, HTA and reducing inequalities.

    In this chapter

    1. MEP questions: competitiveness, advanced therapies and data useGerald Hauser
    2. Minister’s responses: EHDS, innovation, pricing and inequalities

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  18. GMT+2

    Committee on Public Health Ordinary meeting

    Irish Council Presidency: health mandate and priorities

    The Chair introduces the Irish Council Presidency’s health mandate, then MEPs open with questions on safeguarding the EU health budget, shaping the Biotech Act and pharma reform around affordability and access, and addressing AMR, One Health, workforce gaps and health inequalities.

    In this chapter

    1. Introduction of Irish Council Presidency and health mandateAdam Jarubas
    2. MEP questions: health budget, Biotech Act and inequalitiesAdam Jarubas

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  19. GMT+2

    Committee on Public Health Ordinary meeting

    Youth mental health: Triple P introduction and MEP debate

    The Chair opens the agenda item on youth mental health and healthy behaviours, the Triple P expert presents parenting‑focused prevention and related policy implications, followed by MEPs’ questions and remarks on scaling parenting support, regulating digital risks and embedding youth mental health in EU frameworks.

    In this chapter

    1. Chair transition and introduction of Triple P expertAdam Jarubas
    2. Parenting, family environment and Triple P policy implicationsAdam Jarubas
    3. MEP interventions: parenting, youth mental health and digital risksNikos Papandreou

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  20. GMT+2

    Committee on Public Health Ordinary meeting

    Youth mental health study: evidence, costs and EU options

    Presentation of the EPRS ‘cost of non-Europe’ study on youth mental health in the digital era, detailing methodology, prevalence, inequalities, digital risk factors and economic burden, followed by MEPs’ questions and experts’ replies on drivers of ill‑health, COVID and digital harms, EU competences, best practices and priority EU-level policy interventions.

    In this chapter

    1. EPRS youth mental health study: scope, findings, EU policy optionsAdam Jarubas
    2. MEPs’ questions and experts’ replies on EU youth mental healthAdam Jarubas

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  21. GMT+2

    Committee on Public Health Ordinary meeting

    WHO World Health Assembly mission: EU role and WHO reforms

    Report on the SANT delegation’s mission to the 79th World Health Assembly focusing on WHO reform, financing after US withdrawal, the Pandemic Agreement and PABS, and the EU’s political and financial stance, followed by debate on WHO independence, private funding and alleged foundation influence before closing the mission report.

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  22. GMT+2

    Committee on Public Health Ordinary meeting

    US mission mandate and transatlantic health security

    Opening of the SANT meeting, adoption of the agenda and explanation of the committee’s mission to Washington and Pittsburgh, followed by detailed feedback on US health stakeholders, ‘America First’ health policy, global health implications, and risks for EU health systems and access to medicines.

    In this chapter

    1. Opening of SANT meeting and US mission mandateAdam Jarubas
    2. US health stakeholders, policies and implications for EUIgnazio Roberto Marino

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  23. GMT+2

    Committee on Public Health Ordinary meeting Joint meeting Committee on Industry, Research and Energy

    Commission response, SPC defence and meeting closure

    The Commission justifies its proposal, insisting on unchanged safety and ethics, explains the conditional 12‑month SPC incentive and its links with wider pharmaceutical files, while the co‑rapporteurs rebut criticism, restate the Act’s key pillars, outline compromise work and the Chair announces the amendment deadline before closing.

    In this chapter

    1. Commission (DG SANTE): defence of proposal and conditional SPCsThomas Van Cangh
    2. Co‑rapporteurs’ closing remarks and next stepsWouter Beke

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  24. GMT+2

    Committee on Public Health Ordinary meeting Joint meeting Committee on Industry, Research and Energy

    Legal affairs and further MEP views: AI, SPC and workforce

    The JURI rapporteur and catch‑the‑eye MEPs debate ethical and legal safeguards for AI in healthcare, oppose or defend SPC extensions, call for stronger harmonisation of trials, raise concerns about reliance on non‑EU data, and highlight centres of excellence, skills and geographic balance of biotech activities.

    In this chapter

    1. JURI rapporteur Wölken: AI ethics and deletion of SPC extensionTiemo Wölken
    2. Catch‑the‑eye MEPs: harmonisation, SPC, China trials and workforcePeter Liese

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  25. GMT+2

    Committee on Public Health Ordinary meeting Joint meeting Committee on Industry, Research and Energy

    Political group shadows: biotech ecosystem, trials and SPC

    Shadows from EPP, S&D, ID, ECR, Renew, Greens and ENS set out their positions on biotech sovereignty, clinical trial timelines and governance, data protection, IP and SPC extensions, strategic project criteria, ethical safeguards and the balance between industrial incentives, biosimilars and affordability.

    In this chapter

    1. EPP SANT shadow Ter Laak: support for ambition, data and patientsIngeborg Ter Laak
    2. S&D shadow statement: biotech sovereignty, funding and SPC cautionVytenis Povilas Andriukaitis
    3. Patriotes/ID shadow De la Pisa: strategic projects, SMEs and ethicsMargarita de la Pisa Carrión

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  26. GMT+2

    Committee on Public Health Ordinary meeting Joint meeting Committee on Industry, Research and Energy

    Opening and co‑rapporteurs’ Biotech Act mandate

    The Chair opens the joint SANT–ITRE meeting, sets out procedure and context, and the co‑rapporteurs present their strategic vision for the European Biotech Act, focusing on competitiveness, clinical trials reform, data and AI use, EMA’s role and financing tools such as a scale‑up fund.

    In this chapter

    1. Opening, agenda adoption and procedureAdam Jarubas
    2. SANT co‑rapporteur Andriukaitis: Biotech Act vision and pillarsVytenis Povilas Andriukaitis
    3. ITRE co‑rapporteur Beke: industrial focus, trials and scale‑up fundWouter Beke

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Schedule

  1. Replay

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  2. Replay

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  3. Replay

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  4. Replay

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  5. Replay

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  6. Replay

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  7. Replay

    Part 1Part 2

  8. Replay

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  9. Replay

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  10. Replay

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  11. Replay

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  12. Replay

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  13. Upcoming
    Committee on Public Health - Ordinary meeting
  14. Upcoming
    Committee on Public Health - Ordinary meeting
  15. Upcoming
    Committee on Public Health - Ordinary meeting

Who spoke at the committee

  • Adam Jarubas 24 sittings
  • Stine Bosse 20 sittings
  • Vytenis Povilas Andriukaitis 19 sittings
  • Tomislav Sokol 15 sittings
  • András Tivadar Kulja 11 sittings
  • Aurelijus Veryga 11 sittings
  • Catarina Martins 10 sittings
  • Christophe Clergeau 10 sittings
  • Gerald Hauser 10 sittings
  • Tilly Metz 10 sittings
  • Vlad Vasile-Voiculescu 10 sittings
  • Marie-Luce Brasier-Clain 9 sittings
  • Nicolás González Casares 9 sittings
  • Elena Nevado del Campo 8 sittings
  • Ignazio Roberto Marino 8 sittings
  • Margarita de la Pisa Carrión 8 sittings
  • Ondřej Dostál 8 sittings
  • Martin Häusling 7 sittings
  • Laurent Castillo 6 sittings
  • Nikos Papandreou 6 sittings
  • Bartosz Arłukowicz 5 sittings
  • Oliver Schenk 5 sittings
  • Olivér Várhelyi 5 sittings
  • Peter Agius 5 sittings
  • Peter Liese 5 sittings
  • Tiemo Wölken 5 sittings
  • Victor Negrescu 5 sittings
  • Christine Anderson 4 sittings
  • Jessica Polfjärd 4 sittings
  • Leire Pajín 4 sittings

Where these transcripts come from

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47 sittings on Polyfact since 14 May 2025

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