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Tuesday, September 29
 

11:30 CEST

Progress and challenges of advanced therapies for rare diseases
Tuesday September 29, 2026 11:30 - 12:00 CEST
Dr. Bueren leads the Biomedical Innovation Unit at CIEMAT and also conducts research at CIBERER and the Jiménez Díaz Foundation Health Research Institute. Throughout his career, he has made decisive contributions to the development of new gene and cell therapies targeting rare and hereditary diseases, driving the translation of research from the laboratory to clinical practice.

Internationally recognized for his scientific contributions and leadership in the field of gene therapy, he has also served as president of the European Society for Gene and Cell Therapy, promoting the advancement and accessibility of these innovative therapies for patients.

At BIOSPAIN, he will will share an updated perspective on the advances transforming the treatment of rare diseases, as well as the scientific, regulatory, and access challenges that still need to be overcome to ensure these therapies reach all patients who need them.
Speakers
avatar for Juan A. Bueren Roncero

Juan A. Bueren Roncero

Director Biomedical Innovation Unit, Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT)
Head of the Division of Innovative Therapies in the Hematopoietic System at CIEMAT and CIBER of Rare Diseases of the ISCIII, as well as Coordinator of the Joint Unit for Advanced Therapies CIEMAT/IIS-Jiménez Díaz Foundation. Vice President of the ESGCT.
Tuesday September 29, 2026 11:30 - 12:00 CEST
2 Dorotea Barnés room

12:15 CEST

Beyond Discovery: How AI, Advanced Therapeutics and Clinical Evidence Are Reshaping Biotech Innovation
Tuesday September 29, 2026 12:15 - 13:00 CEST
The biotechnology sector is entering a new era in which innovation is no longer driven by scientific discovery alone. The increasing convergence of artificial intelligence, advanced therapeutic approaches, and data-driven clinical decision-making is fundamentally transforming the way new healthcare solutions are conceived, developed, validated, and ultimately delivered to patients. As scientific and technological capabilities continue to evolve, collaboration across disciplines has become essential to accelerate innovation, reduce development timelines, and improve healthcare outcomes.
From the earliest stages of target identification and drug discovery to the generation of clinical evidence that supports regulatory approval, market access, and patient care, biotechnology companies are embracing new technologies that are reshaping every step of the innovation pathway. Artificial intelligence is enabling researchers to analyse complex biological data with unprecedented speed and precision, novel therapeutic strategies are opening new possibilities for treating diseases previously considered undruggable, and real-world data is becoming an indispensable tool for demonstrating the value and effectiveness of healthcare innovations beyond the clinical trial setting.
This session will bring together three innovative companies representing complementary areas of this evolving biotechnology ecosystem. Their experiences will illustrate how cutting-edge science, digital technologies, and clinical evidence generation can work together to create a more integrated, efficient, and patient-centred model of innovation. Through their different perspectives, the discussion will explore how multidisciplinary collaboration is becoming one of the key drivers of competitiveness within the global biotech industry.
Beyond showcasing technological advances, the panel will also address some of the major challenges facing biotechnology companies today, including access to high-quality data, regulatory adaptation to emerging technologies, talent attraction, investment, and the importance of building collaborative innovation ecosystems capable of supporting companies from early-stage research through to market adoption.
The discussion will also provide an opportunity to reflect on Europe's position within an increasingly competitive global landscape. As biotechnology becomes more digital, interconnected, and data-intensive, strengthening collaboration between startups, healthcare providers, research organisations, technology developers, investors, and public institutions will be critical to ensuring that innovation reaches patients faster and more effectively.
This session is designed for biotech entrepreneurs, pharmaceutical and medtech companies, researchers, investors, healthcare professionals, and innovation policymakers interested in understanding how the next generation of biotechnology will be built through the integration of artificial intelligence, advanced therapeutic innovation, and clinical evidence.

Speakers
avatar for Juan Sebastián Ruiz

Juan Sebastián Ruiz

CEO, APTADEGRAD
CEO de Aptadegrad y Lincbiotech.  Licenciado y basado en Madrid/Santiago de Compostela, lidera la spin-off biomédica Lincbiotech  del IDIS especializada en el diagnóstico y tratamiento de enfermedades neurológicas graves (como el Alzheimer y el ictus) utilizando intelige... Read More →
avatar for Alejandro Martí

Alejandro Martí

CEO, Votum Labs
Alejandro Martí, junto a Borja Vera, fundó Votum Laboratorios en 2021 con el objetivo de transformar la salud y el bienestar a través de cannabinoides seguros, eficaces y avalados por la ciencia. En apenas tres años, la empresa ha lanzado varias líneas de producto propias para personas y mascotas, certificado su... Read More →
avatar for Manuel Vielma

Manuel Vielma

CEO, E-PISTEME
Manuel Vielma, CEO y fundador de E-Pisteme, startup edTech de la Comunidad LN, trabajan impulsando el aprendizaje STEM a través de experiencias inmersivas, tecnología y creatividad. Gracias a soluciones como E-Tellurion, su kit interactivo sobre el sistema solar, los estudiantes... Read More →
Tuesday September 29, 2026 12:15 - 13:00 CEST
2 Dorotea Barnés room

14:30 CEST

Boosting biotechnology development accelerators
Tuesday September 29, 2026 14:30 - 15:15 CEST
The Biotech Act will establish the first comprehensive framework to promote biotechnology as a strategic sector for the European Union’s competitiveness, public health, sustainability, and technological autonomy. The law aims to position Europe in the global competition with the United States and China in this strategically important field.
About fostering biotechnology startup companies in the health sector, the Biotech Act outlines the structural conditions and mechanisms needed to accelerate innovation and improve the translation of research into market applications, so that such initiatives may be recognized by the Commission as “high impact health biotechnology strategic projects”.
The Biotech Act advocates for achieving critical mass through clusters - not hundreds of small biotechnology hubs scattered everywhere - but rather half a dozen large “super-clusters” capable of attracting substantial investment and offering strong, competitive capacities in innovation, manufacturing, and infrastructure.

-Lilly, pendiente ponente
Moderators
avatar for Amelia Martín Uranga

Amelia Martín Uranga

Director of Clinical and Translational Research, FARMAINDUSTRIA
Amelia Martín Uranga, PhD in Law, Director of Clinical and Translational Research and Head of the Innovative Medicines Platform (Farmaindustria), focuses primarily on the implementation and management of public-private partnership projects, such as the BEST Project and the Pharma-Biotech... Read More →
Speakers
avatar for María José Lallena Jimeno

María José Lallena Jimeno

Directora del Centro de Investigación, Desarrollo e Innovación, Fundación LILLY
Doctora en Bioquímica y Biología Molecular por la Universidad Autónoma de Madrid. Su trayectoria profesional se inició con dos periodos postdoctorales: el primero de ellos en el Centro de Biología Molecular de Madrid y el segundo, en el Laboratorio Europeo de Biología Molecular... Read More →
avatar for Idoia Muñoz Lizán

Idoia Muñoz Lizán

Managing Director, Basque Health Cluster

avatar for Núria Martí

Núria Martí

Director of Innovation and Business Development, Biocat
Núria Martí Ras has an undergraduate degree in Veterinary Sciences (Autonomous University of Barcelona, 1993), PhD in Veterinary Sciences (UAB, 1999), master’s in Laboratory Animal Science and Welfare (UAB, 2009) and a master’s in R&D Management in Health from the Carlos III... Read More →
avatar for Javier Jiménez

Javier Jiménez

Chief Medical Officer, Pharmamar
Experienced healthcare professional with over two decades of experience leading evidence generation strategies and research at some of the world’s most prestigious pharmaceutical and health technology companies. As Chief Medical Officer at PharmaMar, I drive the integration clinical... Read More →
avatar for Marisol Quintero

Marisol Quintero

COO, Highlight Therapeutics

Tuesday September 29, 2026 14:30 - 15:15 CEST
2 Dorotea Barnés room

14:30 CEST

From Zero to GMP. Built to Scale
Tuesday September 29, 2026 14:30 - 15:15 CEST
Ponentes:
Dámaso Molero
Reprsentante de Sartorius,
Reopresentante de un cliente
Representante de ingeniería
Speakers
avatar for Dámaso Molero Sánchez

Dámaso Molero Sánchez

Group Chief Executive Officer, 3P Biovian
Experienced General Manager with a demonstrated successful history of more than 34 years working in Pharma and Biotechnology industry. Plant Director, Qualified Person and others. Member of Executive Board of ASEBIO (Spanish Asociation of Bio Companies) Member as an expert of "High-Level... Read More →
Tuesday September 29, 2026 14:30 - 15:15 CEST
3 Nicolás Achúcarro room

15:15 CEST

Advanced therapies and next-gen biotech platforms to deliver global health impact
Tuesday September 29, 2026 15:15 - 16:00 CEST
Advanced Therapies and Next-Gen Biotech Platforms to Deliver Global Health Impact
Given the relative strength of the Basque Country in industrial biotechnology capabilities—particularly in advanced manufacturing, regenerative medicine, and translational research—this proposal envisions a coherent set of 2–3 interconnected BIOSPAIN 2026 sessions exploring advanced therapies and next-generation biotech platforms from complementary perspectives. Rather than a single discussion, the aim is to reflect the breadth and maturity of the regional ecosystem by distributing expertise across multiple formats, including thematic panels and moderated discussions.
These sessions would collectively examine how scientific innovation, industrial scale-up, and clinical translation converge to enable global impact in advanced therapies. While each session would address a distinct angle—from platform technologies and manufacturing infrastructure to translational science and clinical application—they would be designed to offer a unified narrative around the Basque Country’s role as a European hub for advanced biomedicine.
Across the proposed sessions, participation would include leading voices from biotechnology companies, industrial-scale manufacturing organizations, and academic and translational research institutions:
The session provides a review of platform technologies and genome engineering, industrialization and manufacturing of gene and cell therapies, and translational research and clinical integration, depending on final program design.
Overall, this proposal aims to showcase the Basque Country’s distinctive positioning at the intersection of industrial capability, scientific excellence, and translational innovation, illustrating how regional strengths can be leveraged to drive global health impact in advanced therapies through coordinated, multi-stakeholder dialogue.

Speakers
avatar for Javier Alonso Gómez

Javier Alonso Gómez

General Manager, Litek Pharma

avatar for Jimmy Vanhove

Jimmy Vanhove

CEO, Viralgen
Jimmy Vanhove brings extensive experience in strategy, operational management, and digital transformation in the biotech/pharma industry. He has held various leadership positions with increased responsibility in manufacturing and strategy consulting at multinational companies like... Read More →
avatar for Julio Font

Julio Font

CEO, Histocell

avatar for Francisco Borrego

Francisco Borrego

Ikerbasque Research Professor at Biobizkaia Health Research Institute, IIS Biobizkaia
I hold a Bachelor's and a Doctorate in Medicine and Surgery from the University of Córdoba. After completing my doctoral thesis, I worked for 18 years in the United States. The first 13 years were at the National Institutes of Health (NIH), and the following 5 years at the U.S. Food... Read More →
Tuesday September 29, 2026 15:15 - 16:00 CEST
2 Dorotea Barnés room

16:00 CEST

AI and quantum computing in drug discovery: transforming molecular design and therapeutic development
Tuesday September 29, 2026 16:00 - 16:45 CEST
Quantum technologies are rapidly evolving from theoretical promise to practical tools across biomedicine and biotechnology. Early applications in drug discovery, molecular simulation, quantum enhanced imaging, and secure data infrastructures are already underway, supported by hybrid quantum–classical approaches and pioneering industrial collaborations. This panel will bring together experts from quantum computing, biotechnology, diagnostics, and cybersecurity to explore near term opportunities and realistic pathways for adoption.
Participants will gain insights into emerging use cases, regulatory considerations, and strategic actions enabling biotech and health organizations to prepare for the quantum decade ahead.

Introduction: Why Quantum for Biotech Now? (5 min)

Block 1 – Quantum Computing in Biomedicine: Molecules, Models and Precision Medicine (20 min)

Block 2 – Quantum Sensing, Imaging and Diagnostics: The Next Frontier (20 min)

Block 3 – Quantum Biotech Industrial Collaborations and Biomanufacturing (20 min)

1. Mujer TBC, Multiverse Computing
2. Javier Aizpurua, Scientific director, BasQ-Basque Quantum Strategy TBC
Moderators
avatar for Aitor Bergara

Aitor Bergara

Professor of Quantum Physics at UPV/EHU and Director of the EHU Quantum Center., University of the Basque Country

Speakers
avatar for David Hallett

David Hallett

Chief Scientific Officer, RECURSION

avatar for Ibai Díez Palacio

Ibai Díez Palacio

Assistant Professor of Radiology /Group coordinator CNS diseases & Computational Imaging, IIS Biobizkaia/Harvard Medical School
am an Instructor of Radiology with advanced neuroimaging, biomedical and computational expertise. My work has focused on developing cutting-edge neuroimaging methods and pipelines for multimodal neuroimage research. My research background combines a wide range of imaging techniques... Read More →
Tuesday September 29, 2026 16:00 - 16:45 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia

16:00 CEST

Women’s health & care as a growing industry
Tuesday September 29, 2026 16:00 - 16:45 CEST
Women specificities in healthcare are gaining importance due to the higher socieconomical status in developed countries and insights from research highlighting sex and gender disparities in the development, prevention and treatment of diseases. As an example, cardiovascular disease remains the leading cause of death among women in the EU, yet it is still under-researched, frequently misdiagnosed, and often undertreated. Understanding women's health requires moving beyond a "one-size-fits-all" medical model to one that recognizes the profound impact of sex and gender on health outcomes and considers the differential needs in prevention and treatment. In parallel, there is a growing high-tech market delivering new healthcare products and services specifically designed for women, the so-called femtech sector, with innovations specifically designed for women’s wellness or care related to diagnostic devices, wearable sensors, etc. This panel will analyze this healthcare paradigm change and the related technological innovations as well as the integration of these aspects into routine clinical workflows by multidisciplinary experts including a cardiologist with expertise in digital health and AI, pharma and femtech companies.
  • Representante de Abbvie –TBC.
  • Representante de Qassay TBC.

Moderators
avatar for Iván Macía Oliver

Iván Macía Oliver

Director of Digital Health & Biomecial Technologies, Vicomtech

Speakers
avatar for Idoia Muñoz Lizán

Idoia Muñoz Lizán

Managing Director, Basque Health Cluster

avatar for Carlos Escobar

Carlos Escobar

Cardiologist and co-founder Cofounder SAMIRA DTx, Hostpital La Paz
Education: Bachelor of Medicine and Surgery from the Autonomous University of Madrid (1993-99). Doctor of Medicine from the University of Alcalá, awarded summa cum laude by unanimous decision (2007).

Professional Experience: Attending Physician in Cardiology at the Ramón y Cajal University Hospital in Madrid from 2006 to February 2008. Attending Physician in Cardiology at the Infanta Sofía University Hospital in San Sebastián de los Reyes, Madrid, from February 2008 to May... Read More →
avatar for Marina Rigau

Marina Rigau

CEO & Co-Founder, MiMARK

Tuesday September 29, 2026 16:00 - 16:45 CEST
2 Dorotea Barnés room

16:45 CEST

Advancing Cell & Gene Therapies: Challenges, Innovation & Market Translation
Tuesday September 29, 2026 16:45 - 17:30 CEST
Cell and gene therapies (CGT) have revolutionised the treatment of many conditions and they continue to attract significant levels of investment. Their development faces unique challenges, ranging from technical complexity, regulation, scaling production, and the requirement of innovative commercialization models. This roundtable will explore how CGT can be effectively translated into innovation that reaches the market, creates value, and improves people’s lives. A range of topics will be covered, with particular emphasis on some key challenges such as response durability, toxicity management, targeting of solid tumours, and the development of robust analytical workflows for functional characterisation, including approaches such as real-time cytotoxicity assays and multimodal cell profiling.



Speakers
avatar for James Cameron

James Cameron

Market Specialist for Cell & Molecular Research, Agilent NLD
James Cameron is a Market Specialist for BioPharma at Agilent Technologies, specializing in advancing cell and molecular research workflows, mRNA analysis, and critical quality attributes. He frequently acts as a moderator and subject matter expert for key industry discussions. 
... Read More →
avatar for Gaël Roué

Gaël Roué

Junior Group Leader, Josep Carreras Leukaemia Research Institute
Me doctoré en 2002 en la Universidad de Caen (Francia) y trabajé entre 2002 y 2004 como postdoc asociado en el Instituto Pasteur (París, Francia). Posteriormente me trasladé al Hospital Clínic de Barcelona (España) para trabajar en la caracterización de terapias nuevas y traslacionales... Read More →
MA

Miguel Angel Campanero

General Manager, Syngoy

Tuesday September 29, 2026 16:45 - 17:30 CEST
3 Nicolás Achúcarro room
 
Wednesday, September 30
 

09:30 CEST

The Clinical Future of Bioprinting: From biofabrication technologies to next-generation regenerative therapies
Wednesday September 30, 2026 09:30 - 10:15 CEST
Bioprinting is rapidly evolving from an emerging laboratory technology into a transformative clinical platform with the potential to redefine regenerative medicine. This roundtable will bring together key European stakeholders from biofabrication, robotics, clinical translation and advanced manufacturing to discuss how bioprinting can successfully move from research environments into real-world medical practice.
Through complementary perspectives, the discussion will address the major challenges and opportunities facing the field: unmet clinical needs, in vivo bioprinting, robotic-assisted biofabrication, industrial scalability, regulatory pathways, hospital integration and next-generation regenerative therapies. The session aims to provide a realistic and strategic vision of how the clinical future of bioprinting can be built.
The roundtable would be moderated by Andrea García Lizarribar (TECNALIA), who will guide the discussion around the technological, clinical and industrial pathways required to accelerate the adoption of biofabrication technologies in healthcare.
The proposed panel creates a strong and complementary storyline around the clinical translation of bioprinting technologies:

  • Enabling technologies and manufacturing platforms → REGEMAT 3D
Together, the panel balances:
  • clinical perspective
  • industrial scalability
  • enabling technologies
  • advanced therapies
  • future-oriented innovation
  • while maintaining a realistic and high-impact discussion on how bioprinting can successfully transition from research laboratories into clinical practice.
The session offers a unique opportunity to showcase how European innovation ecosystems are shaping the future of clinically applicable biofabrication technologies.
Moderators
avatar for Andrea García Lizarribar

Andrea García Lizarribar

Investigadora de Biomateriales de Salud, TECNALIA
Doctora en Biomedicina por la Universidad de Barcelona. Graduada en Biotecnología por la Universidad de Girona en 2015, donde realizó el trabajo de final de grado en el departamento de bioquímica y biología molecular. Obtuvo el Máster en Biotecnología Molecular de la Universidad... Read More →
Speakers
avatar for Francisco Miguel Sánchez Margallo

Francisco Miguel Sánchez Margallo

Director Científico del CCMIJU, Centro de Cirugía de Mínima Invasión Jesús Usón (CCMIJU)
Con más de 30 años de experiencia, el Dr. Sánchez Margallo es el Director Científico del Centro de Cirugía de Mínima Invasión Jesús Usón (CCMIJU), donde ha liderado importantes avances, como la participación del CCMIJU en el primer trasplante pulmonar robótico realizado... Read More →
JM

Jesús María Izco Zaratiegui

Bioproducts Diversification Manager, VISCOFAN

LM

Luc Milbergue

Presidente, POIETIS Biosistems
Luc Milbergue cuenta con experiencia previa en Strategir, Energies & Castors y Base Innovation. Fue Superintendente de Compañía de Burdeos entre 1983 y 1986. Posee una sólida trayectoria profesional que incluye desarrollo de nuevos negocios, ventas, desarrollo de productos, Microsoft... Read More →
Wednesday September 30, 2026 09:30 - 10:15 CEST
2 Dorotea Barnés room

11:30 CEST

From Platform to Patient: Scaling Biotech and Advanced Therapies Through Integrated CDMO Ecosystems
Wednesday September 30, 2026 11:30 - 12:15 CEST
As biologics and advanced therapies—including proteins, antibodies, and ATMPs—reshape the therapeutic landscape, the key challenge is no longer only scientific, but industrial. This roundtable will explore how CDMOs are evolving beyond isolated capabilities into integrated, platform-driven ecosystems that accelerate development, reduce risk, and enable efficient path-to-patient.


Rather than focusing solely on technologies, the discussion will highlight how collaboration across specialized players—viral vector developers, biologics manufacturers, and fill-finish experts—can create seamless development pathways. The goal is to understand how to connect early innovation with robust, scalable, and compliant manufacturing strategies.
Key Discussion Topics
  • Platforms as enablers: How standardized platforms can reduce timelines and costs, while balancing the need for flexibility in complex and novel therapies.


  •  End-to-end thinking: The importance of integrating drug substance and drug product considerations early to avoid late-stage challenges.

  • Scaling advanced therapies: Key bottlenecks in moving from clinical to commercial manufacturing, particularly for ATMPs and viral vectors.

  • The power of proximity: Why close collaboration between CDMO teams and developers is critical to accelerate decision-making, knowledge transfer, and execution.
Differentiation Angle:

This session will provide a strategic perspective on how to move from fragmented innovation to coordinated industrial execution—combining platform efficiency with collaboration—to ultimately deliver complex therapies to patients faster and more reliably.

Moderators
avatar for Andreu Soldevilla

Andreu Soldevilla

CEO, Syna Therapeutics

Speakers
avatar for Laura de la Torre

Laura de la Torre

MK Manager, Leanbio

avatar for Natalia Elizalde

Natalia Elizalde

Chief Business Development Officer, Vivebiotech
Graduate in Pharmacy, she developed her end of degree project at UCLH Hospital in London. Afterwards, she was awarded a European PhD as a result of a thesis (University of Navarra; temporary stay at Oxford University) focused on the long-term effects of chronic mild stress over behaviour... Read More →
avatar for David Blanco Berrenechea

David Blanco Berrenechea

Business Development & Programme Management Director, LeanBio
15 years of experience in biotech and pharmaceuticals business development and project management including PMP certification. Proven business leader with demonstrated success managing global complex CDMO projects in the Pharma and Biotech Industry and integrating all aspects of complex... Read More →
avatar for András Dinnyés

András Dinnyés

Co-founder and General Director, Biotalentum
Co-founder and general director of BioTalentum Ltd. He has been working on embryology, cryobiology, cloning and stem cell biology since 1985. He has been a Fulbright Scholar in the US in 1991-92 and worked at the University of Connecticut (US) for 1997-99, where he invented and patented... Read More →
Wednesday September 30, 2026 11:30 - 12:15 CEST
2 Dorotea Barnés room

12:15 CEST

Can Cooperative Models Transform the Future of Pharma and Healthcare?
Wednesday September 30, 2026 12:15 - 13:00 CEST

Speakers
avatar for Raúl Pérez

Raúl Pérez

Director científico, I+Med.

avatar for Manuel Sánchez-Lagarejo

Manuel Sánchez-Lagarejo

Director general, Bexen Medical & Bexen Bioservices

Wednesday September 30, 2026 12:15 - 13:00 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia

14:30 CEST

Accelerating Oncology Innovation: Collaborative Models for Early Translation
Wednesday September 30, 2026 14:30 - 15:15 CEST
The successful translation of early-stage oncology research into therapies that reach patients requires more than scientific excellence. It demands effective collaboration among researchers, technology transfer professionals, biotech companies, patient organizations, investors, and funding institutions. As Europe increasingly embraces collaborative and impact-driven innovation models, new approaches are emerging to bridge the gap between discovery and clinical application.

This roundtable will explore how structured collaboration can accelerate oncology innovation and improve the likelihood that promising discoveries reach patients. Using real-world examples from the oncology innovation ecosystem, the session will highlight how coordinated support mechanisms can de-risk early-stage projects, strengthen translational pathways, and ensure patient needs are integrated from the outset.
The discussion will address key drivers transforming oncology drug development, including:
  • Advances in molecular biology, genomics, and biomarker-driven clinical development that are enabling more precise and targeted therapeutic strategies.
  • The growing use of real-world data (RWD) and real-world evidence (RWE) to inform clinical development and decision-making.
  • The integration of patient perspectives from the earliest stages of research, ensuring that scientific priorities, development pathways, and innovation outcomes reflect real clinical needs and patient experiences.
  • The application of artificial intelligence and machine learning across the R&D continuum, from target identification and drug discovery to biomarker development, clinical trial optimization, patient recruitment, and prediction of treatment response and toxicity.
Bringing together perspectives from academia, venture capital, biotech SMEs, patient advocacy organizations, and innovation support entities, the session will provide actionable insights into how collaborative ecosystems can accelerate oncology innovation and create greater translational impact.

A particular focus will be placed on the role of innovation support and incubation programs in identifying high-potential research projects and transforming them into investable opportunities. Speakers will discuss how early definition of an investment thesis—grounded in patient benefit, societal impact, and commercial potential—can strengthen project development and attract follow-on investment. The session will also explore how venture capital investors increasingly contribute beyond financing, actively supporting project evaluation, strategic positioning, and market alignment from the earliest stages. AECC, the Spanish Association Against Cancer, will present their pioneering Patient Advocacy programme its complemnetarity to their  newTechnology Transfer Program.

Representatives from Oncomatryx, Naru Intelligence, and Hawk Biosystems will share their experiences in developing cutting-edge technologies, including antibody-drug conjugates (ADCs), AI-driven clinical research solutions, and next-generation spatial proteomics platforms.

By showcasing successful examples of cross-sector collaboration, this session will demonstrate how coordinated innovation ecosystems can accelerate the journey from laboratory discovery to patient benefit.
Participants will gain practical insights into building investable, patient-centered oncology projects and fostering partnerships that accelerate translation and market adoption.


Proposed Panelists
  • Representative, AECC Patient Advocacy Program / AECC INNOVA or AECC IMPACTO initiatives?

Moderators
avatar for Sofía Cabezudo

Sofía Cabezudo

Head of Innovation, Fundación Científica de la Asociación Española Contra el Cáncer

Speakers
avatar for Laureano Simón

Laureano Simón

CEO, Oncomatryx
Dr. Simón is the founder of Progenika Biopharma S.A. and co-founder of Progenika Inc., Proteomika S.L., and Abytnek Biopharma S.L. Dr. Simón has extensive experience in the diagnostics industry and has collaborated successfully with pharmaceutical companies.
Currently, Dr. Simón is the CEO of Progenika Group, co-CEO of Progenika Inc., and serves as a Director in biotechnology companies in Europe and the United States.He also advises various governments, scientific committees, public institutions, and private foundations on technology... Read More →
avatar for Arkaitz Carracedo

Arkaitz Carracedo

ERC Consolidator Grant Ikerbasque Research Professor Cancer Cell Signaling And Metabolism Lab, CIC Biogune
Arkaitz Carracedo obtained his BSc in Biology from the Complutense University of Madrid, and he continued his scientific pursuits by completing his PhD in Biochemistry and Molecular Biology at the same university. At this early stage in his career, he focused on researching the "... Read More →
avatar for Eider Sánchez

Eider Sánchez

Cofounder & CEO, Naru Intelligence Solutions S.L.

avatar for Fernando Aguirre

Fernando Aguirre

CEO, Hawk Biosystems
MSc in Physics, Fernando has more than 25 years of new business launch leadership across business development, internationalization and M&A, both as an entrepreneur (he has founded 5 companies so far) as well as in global management position in multinational companies such as Ericsson... Read More →
Wednesday September 30, 2026 14:30 - 15:15 CEST
2 Dorotea Barnés room

14:30 CEST

Advancing Transplant Innovation: Bridging Clinical Excellence with Smarter Drug Development
Wednesday September 30, 2026 14:30 - 15:15 CEST
A silent storm is sweeping the globe: chronic kidney failure touches more than 850 million lives, ranks ninth among causes of death, and affects roughly 10% of the world’s population. In Spain alone, 15% of adults live with chronic kidney disease and about 68,000 people require dialysis or transplant to survive. Spain stands out as a beacon of transplant medicine — performing more than 6,000 kidney transplants a year and consistently leading the world in donor rates and clinical outcomes. Yet even a success story must evolve. To truly conquer organ shortages, extend long-term graft survival, and free patients from lifelong immunosuppression, bold innovation is essential. The horizon is already changing: xenotransplantation, advanced machine perfusion for organ preservation, robotic-assisted surgery (an area where Spain is a trailblazer), and AI-driven donor–recipient matching are reshaping what’s possible. Transplantation is re-emerging as a frontier of therapeutic invention, offering a rare opportunity to recast how drugs and biologics are developed for complex, high-stakes indications. Spain’s dense, high-volume clinical landscape offers an exceptional proving ground to accelerate next-generation drug development. By weaving together model-informed drug development, adaptive and innovative trial designs, and early regulatory alignment, we can shorten timelines, reduce development risk, and create more efficient clinical programs. The complexity of transplant studies — patient heterogeneity, long timelines, and shifting endpoints — demands this kind of nimble, collaborative approach. What’s needed now is stronger partnership between clinical centers, industry, regulators, and patient organizations to build an integrated ecosystem for transplant-focused innovation. The upcoming round table will explore how Spain can leverage its clinical excellence to become a global reference for transplant drug development, and how a forward-looking, coordinated strategy can turn today’s promise into tomorrow’s cures.
Speakers
avatar for Isabel Portero

Isabel Portero

CSO & Founder, Biohope
Isabel Portero (Salamanca, 1970) is the founder and CEO of Biohope, a startup dedicated to the creation and development of biomedical tests that allow for personalized medical treatment in diseases with an immunological basis. A Doctor of Medicine and specialist in Internal Medicine... Read More →
avatar for Alberto Breda

Alberto Breda

Head of Urologic Oncology and the Renal Transplant Surgical Team, Fundació Puigvert
Deputy Director of the Urology Department | Puigvert FoundationThis position is combined with the direction of the Urologic Oncology Unit and the Renal Transplant Surgical Team. Puigvert Foundation, Barcelona.
President of the Robotic Surgery Section | European Robotic Urology Sec... Read More →
avatar for Beatriz Dominguez-Gil

Beatriz Dominguez-Gil

General Director, National Transplant Organization (ONT)
Beatriz Domínguez-Gil holds a degree in Medicine and Surgery from the University of Salamanca. She earned her doctorate in Internal Medicine from the Complutense University of Madrid and worked as a nephrologist at the 12 de Octubre Hospital in Madrid from 2000 to 2007.Before being appointed director of... Read More →
avatar for Sofía Zárraga Larrondo

Sofía Zárraga Larrondo

Jefa de Servicio de Nefrología en Hospital Universitario de Cruces (Osakidetza)

TS

Tim Schroeder

CEO, CTI Clinical Trial & Consulting
Tim is Executive Chairman and Founder of CTI, bringing more than 35 years of clinical, academic, and industry experience in global drug and device development. Prior to founding CTI, he held numerous faculty positions at the University of Cincinnati College of Medicine. Tim was also... Read More →
Wednesday September 30, 2026 14:30 - 15:15 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia

16:00 CEST

Advances in Neurodegenerative Diseases: From Novel Therapies to Real-World Clinical Validation
Wednesday September 30, 2026 16:00 - 16:45 CEST
Neurodegenerative diseases such as Amyotrophic Lateral Sclerosis (ALS), Multiple Sclerosis (MS), and Alzheimer's Disease continue to pose major scientific, clinical, and societal challenges. At the same time, unprecedented advances in molecular biology, drug discovery, biomarkers, precision medicine, and advanced therapeutic approaches are transforming the landscape of neurological research and care.

This round table will bring together leading experts from academia, biotechnology, and clinical practice to discuss the latest innovations driving the development of next-generation therapies for neurodegenerative disorders. The discussion will explore emerging therapeutic strategies, including novel small molecules, biologics, regenerative and gene-based approaches, as well as the critical role of translational research in accelerating their path to patients.
Participants will examine how cutting-edge discoveries are being validated through clinical studies and real-world evidence, addressing key challenges related to efficacy assessment, biomarker development, patient stratification, regulatory pathways, and long-term outcomes. Particular attention will be given to lessons learned across ALS, MS, and Alzheimer's disease, highlighting opportunities for cross-disciplinary collaboration and innovation.

Featuring insights from Adolfo López de Munain, representatives of Golden Gait Biotech and CIC bioGUNE, and Ana Martínez Gil, the session will provide a comprehensive perspective on how scientific breakthroughs are advancing from the laboratory to clinical validation and, ultimately, to improved patient outcomes.

Key themes:
  • Advanced therapeutic approaches for ALS, MS, and Alzheimer's disease
  • Translational pathways from discovery to clinical application
  • Biomarkers and patient stratification for precision neurology
  • Clinical trial innovation and real-world evidence generation
  • Collaboration between academia, healthcare systems, and biotech companies
  • Future opportunities and challenges in neurodegenerative disease treatment development
This discussion will offer attendees a unique opportunity to gain insights into the evolving neurodegenerative disease ecosystem and the strategies shaping the next generation of therapeutic innovation.

Speakers

Mónica Povedano, Hospital Univ. Bellvitge, Neurology Service, TBC
Quimatryx, TBA
BMS?
Speakers
avatar for Antonio Oliviero

Antonio Oliviero

CMO, Golden Gait Biotech

Dr. Antonio Oliviero career started in Rome (Catholic University) where he obtained the degree in Medicine (Oct 1993) and the degree in Neurology (Oct 1997). In the same University, Dr Oliviero obtained the PhD in Neuroscience (Jan 8th, 2002). The main research fields of Dr... Read More →
avatar for Adolfo López de Munain

Adolfo López de Munain

Miramoon Pharma & SEED-ALS coordinator/leader, Osakidetza, IIS Biogipuzkoa, Miramoon Pharma
Dr. López de Munain is Chief Scientific Officer and Co-Founder of MiramoonPharma, with over 35 years of experience in clinical neurology, neurogenetics,and translational neuroscience. He holds an MD and a PhD in Medicine from theUniversity of Navarra, where he conducted his doctoral... Read More →
avatar for Ana Martínez Gil

Ana Martínez Gil

Cofounder, Molefy Pharma
Experta en descubrimiento de fármacos y química medicinal, con más de 25 años de experiencia en enfermedades neurodegenerativas. Es profesora de investigación en el CIB-CSIC y cofundadora de Molefy Pharma.
Wednesday September 30, 2026 16:00 - 16:45 CEST
2 Dorotea Barnés room

16:45 CEST

From Biotechnology to Clinical Intelligence: How to Build Biotech Solutions Powered by Software and AI, Interoperable by Design in Europe. Practical case: use in histopathology for biomarker identification
Wednesday September 30, 2026 16:45 - 17:30 CEST
The integration of biotechnology, software, and artificial intelligence is redefining the development of advanced solutions for diagnosis, patient stratifica on, and precision medicine. However, the effective transla on of these innovations into the European clinical environment requires going beyond analytical performance or the experimental validation of biomarkers. It also requires the ability to design robust, interoperable, and regulatorily aligned systems capable of integrating into complex and highly standardized healthcare ecosystems.

This round table will examine how to build biotech solutions powered by soware and AI under an interoperability-by-design approach, incorporating from the earliest stages aspects such as data architecture, semantic standardization, traceability, algorithmic governance, and regulatory compliance. In the European context, frameworks such as the European Health Data Space (EHDS), the AI Act, and the regulations applicable to medical devices and in vitro diagnostics (MDR/IVDR) are shaping a new paradigm in which evidence generation, data quality, and the capacity for technical and semantic integra on are inseparable from clinical value and market viability.

As a practical case, the presentation will address the use of AI in digital histopathology for biomarker iden fica on, an area of par cular relevance due to its poten al in precision oncology and its high methodological complexity. The combina on of digital imaging, computational analysis, and correla on with molecular and clinical data makes it possible to move toward more reproducible and scalable models of ssue characteriza on. However, its effective implementation depends on the harmonization of formats, pre-analytical and analytical quality, clinical validation, and interoperability with pathology systems, electronic health records, and biomedical data platforms. Innovation in AI-based biotechnology cannot be understood solely as an algorithmic challenge. Interoperability is no longer an IT project; it is strategic infrastructure for enabling European biotech to scale with AI.

AEMPS???
Moderators
avatar for Carmen Martín González

Carmen Martín González

CEO, Founder & Sr Principal Consultant, Cmg Meddev SL

Speakers
avatar for Valery Naranjo

Valery Naranjo

CTO, ARTIKODE
Experience as professor, researcher and director of CVBLab. Cordination of European projects. Innovation awards, Technology Transfer to Industry.
Catedrática de Teoría de la Señal. Universidad Politécnica de Valencia. Directora de CVBLab. Área de investigación: inteligencia artificial, análisis de imagen, visión por computador, análisis de señal... Read More →
avatar for Anna Rosés

Anna Rosés

Head of Innovation, Hospital Clínic de Barcelona
I lead innovation with a clear focus: turning complex ideas into execution and real-world impact.

My career spans private sector, entrepreneurship and healthcare, across multinational companies, startups and innovation-driven environments. This path has shaped how I work: combining strategic thinking with a strong execution mindset, moving comfortably in ambiguity, aligning diverse... Read More →
MM

Marta Montilla

Senior Global Quality & Regulatory Affairs Leader, CMG MedDev
Quality and Regulatory Leader with 12+ years of international experience in healthcare and in-vitro diagnostics (IVD), integrating R&D, quality, and regulatory frameworks. Skilled in translating complex regulations into internal policies, implementing operational digital systems... Read More →
Wednesday September 30, 2026 16:45 - 17:30 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia
 
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