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Tuesday, September 29
 

10:15 CEST

Biologics as Strategic Capability: Europe's Production Base in a New Security Era
Tuesday September 29, 2026 10:15 - 11:00 CEST
The ongoing challenges at Europe's borders and beyond, the lingering effects of COVID-19, and the shifting landscape of biological threats have fundamentally reshaped the way Europe must approach its biologic sector. Vaccines, therapeutics, and diagnostics are no longer just healthcare solutions, they are essential strategic assets. Europe's ability to produce these tools quickly, at scale, and on home soil has become a cornerstone of both defense and crisis resilience.

This session brings together key leaders from Europe’s defense, health security, and intelligence sectors to tackle a crucial question: What infrastructure, coordination, procurement strategies, and alliance frameworks does Europe need to ensure its biologics production meets the demands of future crises? By leveraging lessons from recent events and the strategic insights currently driving EU and national plans, panelists will evaluate Europe’s manufacturing readiness, the strategic role of stockpiles, the integration of intelligence in preparedness, and the necessary public-private collaboration to turn strategic goals into operational capabilities.
Speakers
avatar for Maria Christina Stavridou

Maria Christina Stavridou

Head of Vaccine & Immunisation Programmes Commercial, Vaccines & Countermeasures Delivery Chief Operating Officer Group, UKHSA (UK Health Security Agency)
Economist and public sector leader with experience across government, multilateral organisations, and consulting/advisory roles in 10+ countries. I currently lead vaccine planning and supply within the UK’s routine immunisation programmes, overseeing procurement, stock management... Read More →
avatar for Carlota Gómez de la Hoz

Carlota Gómez de la Hoz

Chief Corporate Affairs & Sustainability Officer, LABORATORIOS HIPRA S.A.

avatar for Ceri Morgan

Ceri Morgan

Trade Commissioner Europe, Department for Business and Trade (UK Government)
Ceri Morgan is His Majesty’s Trade Commissioner for Europe, with responsibility for encouraging trade and investment between the UK and other European countries, as well as Israel. In her most recent position, she led the Department for Environment, Food and Rural Affairs... Read More →
avatar for Tomasz Husak

Tomasz Husak

Director for Defence Policy, DG DEFIS (Defence Industry and Space - European Commission)
Tomasz Husak is Director of Directorate A – Defence Policy in the Directorate General for Defence Industry and Space (DG DEFIS) since 16 February 2026. Husak has 20 years of experience in defence and space policy, economics and international relations. Prior to joining the Commission... Read More →
Tuesday September 29, 2026 10:15 - 11:00 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia

10:15 CEST

From Strategy to Collective Action: Building Europe's Agri-Food Biotech Ecosystem Together
Tuesday September 29, 2026 10:15 - 11:00 CEST
Europe has no shortage of ambitious strategies for biotechnology. The challenge now is implementation.
Delivering a competitive, resilient and sustainable European agri-food biotechnology ecosystem will require coordinated action across industry, startups, academia, investors, farmers, policymakers and innovation organisations. No single stakeholder can deliver this transformation alone.
This roundtable will build on the key insights and recommendations collected by the EU Agri-Food Biotech Alliance from representatives from across the entire value chain—including the European Commission, EFSA, industry leaders, startups, investors, research organisations, farmers, retailers and ecosystem partners—to identify the priorities and actions needed to accelerate biotechnology adoption in Europe.
The discussion will focus on how organisations can work together to reduce fragmentation, align around common priorities, launch collaborative initiatives and create greater impact through collective action. The session will conclude with a call for organisations across the value chain to join the effort and help shape a stronger, more connected European agri-food biotechnology ecosystem.


Moderators
avatar for Lorena Savani

Lorena Savani

EIT Food Director of Biotech and Protein Thematic Leadership, EIT Food

Speakers
avatar for Angela Sessitsch

Angela Sessitsch

Head of Health & Bioresources, AIT Austrian Institute of Technology

avatar for Patricia Larráyoz Lorea

Patricia Larráyoz Lorea

Spain’s AgriFoodTech Sandbox Manager, CNTA

Tuesday September 29, 2026 10:15 - 11:00 CEST
3 Nicolás Achúcarro room

11:30 CEST

Choosing the Basque Country to grow your business in life sciences and health – discover the reasons
Tuesday September 29, 2026 11:30 - 12:15 CEST
Since the launch of the BioBasque strategy in 2002, Euskadi has invested in consolidating an innovation ecosystem which supports the growth of the health and life sciences industry. Under the overarching strategy of clusters as models for growth of sophisticated sectors, a sustained institutional support and the public-private collaboration have leveraged the development of a growing industry currently comprised of more than 300 companies (including specialised suppliers) that account for more than 8% of the direct employment in the Basque Country. The industry is also supported and accompanied by the Basque Network of Science, Technology and Innovation, composed of a rich tissue of organisations (Universities, BERC, Cooperativa Research Centres-CIC, Technology Centres gathered in BRTA, and Health Research Institutes among others) which provides skilled capabilities and contribute to generate deeptech start ups.


Since 2015, the industry has experienced very significant growth in the number of companies (60%), and particularly in terms of turnover (187%) and employment (151%). Most of this growth has been endogenous; even today, the generation of innovative and tech companies in the health/life sciences area remains strong (first in Spain, in number of companies per capita). However, in the recent past, the region is becoming an attractive location for companies, and people, that decide to relocate or establish operations and grow their business here.


This session will explore the factors that make the Basque Country attractive, from different points of view including international companies, investors, and researchers, as well as the Basque Health Cluster and the health public administration.

Eikonoklastes Therapeu cs, TBC 



Moderators
avatar for María Aguirre

María Aguirre

Head of Health and Sociohealth transition, SPRI

Speakers
avatar for Fermin Goytisolo

Fermin Goytisolo

Founder ITUA H., Eikonoklastes Therapeutics / ITUA HEALTH

avatar for Lourdes Basabe

Lourdes Basabe

Principal Investigator. Leader of the BIOMICs microfluidics Team, University of the Basque Country
Independent researcher interested in the field of micro bioengineering and lab-on-a-chip technologies. Ikerbasque Research Professor since 2012, Director of the Microfluidics & BIOMICS Cluster UPV/EHU since 2019, Principal Investigator of the BIOMICS-microfluidics Research team since... Read More →
avatar for Iñaki Gutiérrez Ibarluzea

Iñaki Gutiérrez Ibarluzea

Director of Health Research, Innovation and Evaluation, Health Service of the Basque Country

avatar for Javier García Cogorro

Javier García Cogorro

General Partner, Columbus Venture Partners
Founding Partner at Columbus Venture Partners, Javier García spent 25 years at Eli Lilly and Company, where he held various executive positions in Business Development and Information Systems. Since 2009, he has focused on venture capital investment, particularly in private comp... Read More →
avatar for Idoia Muñoz Lizán

Idoia Muñoz Lizán

Managing Director, Basque Health Cluster (BHC)

Tuesday September 29, 2026 11:30 - 12:15 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia

11:30 CEST

What’s the Secret Sauce Behind a Successful Spin-off?
Tuesday September 29, 2026 11:30 - 12:15 CEST
Key success factors behind high-performing spin-offs, including team, science, funding strategy and execution. What to take into account in the early stages to move fast, de-risk projects and build strong foundations for growth. Insights and lessons learned from real cases and different stakeholder perspectives.
Moderators
avatar for Anna Bellmunt

Anna Bellmunt

Senior Associate, Asabys Partners
Senior Associate at Asabys, where she joined in 2021, Anna is responsible for sourcing and assessing opportunities from the scientific, development and business perspectives. Anna currently serves as a board observer at Ona Therapeutics and Nuage Therapeutics.Previously, Anna was... Read More →
Speakers
avatar for Agnés Arbat

Agnés Arbat

Spanish biotech founder, Oxolife

avatar for Gustavo Fuster

Gustavo Fuster

IP lawyer, Hoffmann Eitle
Gustavo Fúster is a patent professional with over 15 years of experience within the field of life sciences patents.

Gustavo first worked as an in-house IP manager and patent specialist in a Spanish biotech firm which provided him with experience in the field of monoclonal antibod

... Read More →
avatar for Etienne Drouet

Etienne Drouet

Vice President, Client Partner & Adviser for Biotech & Venture Capitals, IQVIA
33 years experience in Drug Development in Pharmaceutical industry, Biotech, Contract Research Organisation and Investigational Cooperative Groups.

Specialties: 
- Drug Development in Biotechnology, Oncology, precision medicine & gene therapy, Early Phase Development,
- Project Man



... Read More →
avatar for Marcos Simón

Marcos Simón

Head of TTO, CIC Biomagune

Tuesday September 29, 2026 11:30 - 12:15 CEST
4 Raúl Martín 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.

Moderators
AG

Andrea García Vicente

Director, ABIOINNOVA

Speakers
avatar for Teresa Ruiz Herrero

Teresa Ruiz Herrero

Associate Director Digital Health and RWE, Almirall
I am a dynamic leader and interdisciplinary scientist with over a decade of experience driving innovation at the intersection of technology, healthcare, and strategy. My expertise spans computational modeling, digital health, biomarker discovery, and forging strategic partnerships... Read More →
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

12:15 CEST

Europe’s Biotech Moment: What the Biotech Act Must Deliver
Tuesday September 29, 2026 12:15 - 13:00 CEST
The year 2025 has been marked by the Biotech Act, the proposed Regulation through which the European Commission aims to establish a comprehensive regulatory framework to foster investment, innovation, and competitiveness in the biotechnology sector at a pivotal moment for Europe's strategic autonomy.
Against this backdrop, this session will explore how the Biotech Act represents an opportunity to strengthen the competitiveness of the Spanish biotechnology sector. In particular, the discussion will focus on some of the proposals expected to have the greatest impact on the industry, including Strategic Projects, financing pilots, the extension of the Supplementary Protection Certificate (SPC), and measures to accelerate clinical trials.



Moderators
avatar for Laura Pellísé

Laura Pellísé

Government Affairs Director, Amgen

Speakers
avatar for Cristina Nadal Sanmartin

Cristina Nadal Sanmartin

Executive Director of Policy / President of AseBio, MSD
President of AseBio since December 2025.
Since July 2020, she has held the position of Executive Director of Policy & Government Affairs at the pharmaceutical company Merck, Sharp & Dohme de España, S.A.
Since December 2023, she has been Second Vice President of the Spanish Asso... Read More →
avatar for Javier Padilla Bernáldez

Javier Padilla Bernáldez

Secretary of State, Ministry of Health

Tuesday September 29, 2026 12:15 - 13:00 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia

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.

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

Director of the Research, Development and Innovation Center, Lilly España
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 (BHC)

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
Tuesday September 29, 2026 14:30 - 15:15 CEST
The Decisions Behind Long-Term Success

Twenty years ago, 3PBIOVIAN was founded with a clear purpose: to advance global health by helping innovators bring new therapies to patients. Today, the company is a GMP manufacturing partner supporting healthcare innovators around the world.
What happened in between was neither luck nor a straight path to success. It was the result of deliberate decisions made over two decades of growth, transformation, and execution.
This roundtable explores the critical choices that enable biotechnology companies to move from scientific promise to industrial reality. Bringing together perspectives from an industry leader, a trusted customer, a quality and regulatory expert, and a growth investor, the discussion will examine the decisions that shaped the journey from startup ambition to international scale.
The conversation will explore the thinking behind those choices: setting a long-term strategic direction, building enduring customer partnerships, establishing a quality culture capable of meeting the highest regulatory standards, and securing the financial foundations required for sustainable growth.
This is a conversation about growth, resilience, and the decisions that turn ambition into lasting impact.
Moderators
avatar for Elena Erroba Esquiroz

Elena Erroba Esquiroz

Chief Commercial Officer, 3PBiovian

Speakers
GD

Guido Dietrich

External Consultant

avatar for Javier López Moras

Javier López Moras

Partner, Keensight Capital
Javier is a Partner at Keensight Capital, where he focuses on covering the Spanish market.Prior to Keensight, Javier spent almost 10 years as an M&A advisor in Madrid and London at DC Advisory where he was a Director in the Financial Sponsors & Debt Advisory Practice. He was responsible... Read More →
avatar for Dámaso Molero Sánchez

Dámaso Molero Sánchez

Group Chief Executive Officer, 3PBiovian
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

14:30 CEST

Joint Opportunities for the UK and Spain through Horizon Europe Collaborations.
Tuesday September 29, 2026 14:30 - 15:15 CEST
As the Guest Nation of BIOSPAIN 2026, the United Kingdom takes centre stage in this high-level round table exploring how UK–Spain collaboration can drive innovation, competitiveness and growth across the life sciences sector through Horizon Europe.

Bringing together leading British and Spanish voices from across biotech, research, innovation and public-sector collaboration, this session will examine the strategic value of stronger bilateral partnerships within the Horizon Europe framework. Speakers will discuss how organisations in both countries can work together more effectively in R&D, translational science, health innovation, industrial biotech and international consortia-building.

The discussion will highlight practical pathways for collaboration between UK and Spanish stakeholders, showcase examples of successful partnership models, and explore how both countries can leverage their complementary scientific strengths, innovation ecosystems and shared ambitions to unlock new opportunities in European funding and cross-border innovation.

The round table will offer attendees a timely opportunity to hear directly from experts and decision-makers on the future of UK–Spain cooperation in biotech and the wider life sciences landscape, while celebrating the UK’s special role at BIOSPAIN 2026.

Speakers
avatar for Marcel de Matas

Marcel de Matas

Founder & Chief Business Officer, Seda Pharmaceutical Development & Clinical Manufacturing Services
Marcel is Founder and Chief Business Officer at Seda, a company focussed on delivering chemistry manufacturing and controls (CMC) and clinical pharmacology services. The company is located in Cheadle, Stockport and supports companies across UK, Europe, US, Asia and Australia.

Marcel has led the growth of technical capabilities and services at Seda, and has been instrumental in its transformation from a consultancy based business to an internationally recognised contract research, development, and manufacturing organisation. Services include the development

... Read More →
avatar for Ceri Morgan

Ceri Morgan

Trade Commissioner Europe, Department for Business and Trade (UK Government)
Ceri Morgan is His Majesty’s Trade Commissioner for Europe, with responsibility for encouraging trade and investment between the UK and other European countries, as well as Israel. In her most recent position, she led the Department for Environment, Food and Rural Affairs... Read More →
Tuesday September 29, 2026 14:30 - 15:15 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia

14:30 CEST

Spanish biotech spin-offs and their integration into the global ecosystem: reaching out and attracting EU, US and Asia players
Tuesday September 29, 2026 14:30 - 15:15 CEST
Spanish biotech spin-offs are stepping onto the global stage like nimble launchpads of innovation, pulling in investors and partners from Europe, the US and Asia. Rooted in world-class science yet built for translation, they marry academic brilliance with entrepreneurial grit — and with sharper international branding, smoother regulatory pathways and bolder cross-border alliances, they can turn local discoveries into scalable, globe-spanning solutions.
Moderators
avatar for Emilio Erazo Fischer

Emilio Erazo Fischer

Operating Partne, Asabys Partners
Operating partner at Asabys, Emilio joined the team in December 2024. Emilio supports our biopharma portfolio investments in strategy and business development and currently holds the CBO role at ALLOX.Previously, Emilio led external innovation deals at Boehringer Ingelheim, as Director of Global BD&L Oncology, contributing novel pipeline assets and technology platforms. Emilio has fostered pharma-biotech relationships across Europe, the US and Japan, and served as consultant for... Read More →
Speakers
avatar for Hakan Goker

Hakan Goker

Managing Director, Merck Ventures B.V.
Hakan Goker, PhD, is Managing Director of M Ventures and heads the Biotechnology Investments covering Healthcare and Life Sciences. Hakan joined M Ventures in 2013 and has been investing in the sector for 18 years. Previously, Hakan was a partner at Aescap Venture investing in European... Read More →
avatar for Marc Martinell

Marc Martinell

CEO, Minoryx Therapeutics
Marc Martinell is the founder and CEO of Minoryx Therapeutics, a Spanish biotechnology company specializing in the development of innovative treatments for rare diseases of the central nervous system (CNS). Martinell has also worked at other companies in the sector, such as Oryzon... Read More →
avatar for Alice Zhang

Alice Zhang

Senior Director Strategy, WuXi AppTec

avatar for Prabhu Velusami

Prabhu Velusami

Senior Director S&E EMEA, Johnson & Johnson
Dr Prabhu Velusami is Senior Director of New Ventures and Transactions for Johnson & Johnson Innovation and is located in the Innovation Centre in London. He leads the identification and sourcing of early stage transformative innovation, and the subsequent shaping and execution of... Read More →
Tuesday September 29, 2026 14:30 - 15:15 CEST
4 Raúl Martín 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.

Moderators
avatar for Idoia Muñoz Lizán

Idoia Muñoz Lizán

Managing Director, Basque Health Cluster (BHC)

Speakers
JO

Julen Oyarzabal

CSO & Site Head, Artis Biosolutions

avatar for Virginia Arechavala

Virginia Arechavala

Group Leader Nucleic Acid Therapeutics, IIS Biobizkaia
Currently Works at the Neuromuscular Disorders Group, Biobizkaia Health Research Institute.Research line: Advanced therapies for neuromuscular disorders: antisense oligonucleotides, RNA therapy.Miguel Servet Fellowship I and II, Institute of Health Carlos III, Spain, 2013-2021... Read More →
avatar for Ander Izeta

Ander Izeta

Personalised Medicine and Advances Therapies director, IIS Biogipuzkoa/ Osakidetza/Basque Health Service
Head of a consolidated research group at the BioGipuzkoa Health Research Institute (IIS BioGipuzkoa) and director of the Personalized Medicine and Advanced Therapies Area at BioGipuzkoa. Head of the Advanced Therapies Unit at the Donostialdea Integrated Health Organization (OSI Donostialdea-Donostia... Read More →
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

Tuesday September 29, 2026 15:15 - 16:00 CEST
2 Dorotea Barnés room

15:15 CEST

AI and quantum computing in drug discovery: transforming molecular design and therapeutic development
Tuesday September 29, 2026 15:15 - 16:00 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)

Speakers TBA
Multiverse Computing
BasQ 
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 15:15 - 16:00 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia

15:15 CEST

Bizkaia, an entrepreneurial region: building instruments to boost strategic sectors
Tuesday September 29, 2026 15:15 - 16:00 CEST
Bizkaia has developed its own model for promoting strategic sectors, based, on the one hand, on the territory's capacity to design and activate advanced tax instruments, and on the other hand, on the creation of new financing vehicles that combine private contributions or facilitate access to cutting-edge enabling technologies.

In this round table, representatives from the Bizkaia Provincial Treasury, Seed Capital Bizkaia, BEAZ, and Lank will share how the territory has built specific tools to accelerate innovation and generate new opportunities in sectors such as biotechnology, combining tax incentives, specialized public investment, and future-oriented technological strategies like BIQAIN.









Moderators
avatar for Olatz Goitia Urquiaga

Olatz Goitia Urquiaga

General Director, BEAZ

Speakers
OU

Óscar Ugarte

General Manager, Seed Capital Bizkaia

VG

Valentín García

I+D Director, Lantik

avatar for Idoia Quintanilla

Idoia Quintanilla

Deputy Director of Inspection - Department of Finance, Diputación Foral de Bizkaia

Tuesday September 29, 2026 15:15 - 16:00 CEST
3 Nicolás Achúcarro room

16:00 CEST

AI Driving the Next Generation of Drug Development
Tuesday September 29, 2026 16:00 - 16:45 CEST
Artificial intelligence is reshaping every stage of the pharmaceutical innovation pathway, from the identification of novel therapeutic targets to clinical development, regulatory decision-making and patient access. The convergence of next-generation sequencing, integrative multi-omics, advanced machine learning and emerging European health data infrastructures is creating unprecedented opportunities to accelerate the development of safer, more effective and more personalized medicines.

This round table will gather leaders from government, biotechnology, the pharmaceutical industry and biomedical research to explore how AI is transforming the entire drug development continuum. The discussion will examine how next-generation sequencing and the integration of genomics, transcriptomics, proteomics, metabolomics and other complementary data sources are enabling a deeper understanding of disease biology, improving target identification and validation, and advancing biomarker discovery for precision medicine.

The conversation will then address the application of AI throughout clinical development, including trial design, patient stratification, digital endpoints, real-world evidence generation and regulatory science. Particular attention will be given to the opportunities created by the European Health Data Space (EHDS), which will provide an unprecedented framework for the secure and responsible secondary use of health data to support biomedical research, innovation and evidence generation across Europe.

Beyond the technological advances, the panel will discuss the governance, interoperability and trust frameworks required to translate AI into clinical and societal value. Speakers will also consider how emerging European policy initiatives, including the forthcoming European Biotech Act, can strengthen Europe's innovation ecosystem by fostering investment, enabling responsible data sharing, supporting regulatory innovation and reinforcing the continent's competitiveness in AI-enabled biotechnology.

Bringing together perspectives from industry, academia and public administration, this session will offer a strategic discussion on how Europe—and Spain in particular—can leverage artificial intelligence, integrative 'omics and health data to accelerate biomedical innovation while ensuring scientific excellence, regulatory confidence and better outcomes for patients.



Speakers
avatar for Antonio Fernández-Campa García-Bernardo

Antonio Fernández-Campa García-Bernardo

Manager, Health Knowledge Agency (ACIS)

GJ

Gonzalo Jiménez-Osés

Ikerbasque Research Professor & Principal Investigator, CIC bioGUNE

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

Engineering the Materials of Life
Tuesday September 29, 2026 16:00 - 16:45 CEST
Engineered living materials (ELMs) are composed, either entirely or partly, of living cells. ELMs entirely composed of living cells are called biological ELMs and they self-assemble via a bottom-up process – e.g. synthetic morphogenesis for organoids’ production. ELMs only partly composed of living cells are called hybrid living materials (HLMs) and are built with a top-down process with integrated polymers or scaffolds. In both cases, the cellular components extract energy from the environment to form or assemble the material itself, and to adapt its morphology and function to environmental stimuli. This endows these materials with a combination of properties not present in any non-living material: self-regeneration, adaptation to environmental clues, longevity and environmental sustainability. By being alive, ELMs represent a fundamental change in materials’ production and performance, enabling new, better or similar functionalities, compared to traditional materials but with decreased costs and environmental impact. ELMs have the potential to transform virtually every modern endeavour from healthcare to infrastructures to transportation.


Possible speakers
  • Biotech Alliance members
Speakers
avatar for Manuel Salmeron Sanchez

Manuel Salmeron Sanchez

ICREA Research Professor / IBEC Director, IBEC (Institute for Bioengineering of Catalonia)
Manuel Salmerón-Sánchez es Profesor de Investigación ICREA y Director interino del Instituto de Bioingeniería de Cataluña (IBEC), cargo que asumió en enero de 2026. Es bioingeniero experto en biomateriales avanzados para ingeniería celular y medicina regenerativa.
Cargo act... Read More →
Tuesday September 29, 2026 16:00 - 16:45 CEST
3 Nicolás Achúcarro room

16:00 CEST

Making ATMPs Sustainable in 2026: What Gets Funded, Scaled, and Acquired?
Tuesday September 29, 2026 16:00 - 16:45 CEST
Following a market correction, ATMPs are entering a more selective phase where scientific promise must be matched by clear execution. This session will examine what differentiates companies that get funded, scaled, and ultimately acquired. The discussion will focus on investor selection criteria at seed and Series A, including data thresholds, platform differentiation, and capital efficiency. It will also address the role of delivery and manufacturing in enabling—or limiting—scalability. From a pharma perspective, the panel will highlight what drives partnering and acquisition decisions, and why many ATMP companies fail to reach that stage. Bringing together investors, founders, pharma, and manufacturing experts, the session will provide a practical framework to assess ATMP opportunities in today’s environment.
Moderators
avatar for Robert Fabregat

Robert Fabregat

CEO, BIOCAT
Robert Fabregat (Barcelona, 1980) holds a degree in Chemistry and a PhD in Pharmacy from the University of Barcelona (UB), as well as a Master’s degree in Project Management from BES-La Salle and specific training in Strategy and Innovation from ESADE. From 2019 to 2021, he was... Read More →
Speakers
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 →
avatar for Anna Sanramón Giménez

Anna Sanramón Giménez

Manager, VINCES
Anna presta asesoramiento estratégico en asuntos públicos en el ámbito político, legislativo y social a empresas del sector de la salud.Antes de unirse a Vinces, realizó prácticas profesionales en el Ministerio de Asuntos Exteriores, Unión Europea y Cooperación. Posteriormente... Read More →
avatar for Avencia Sánchez Mejías

Avencia Sánchez Mejías

CEO & Co-founder, Integra Therapeutics
Proud to be leading Integra Therapeutics, a biotech company that is creating next-generation gene writing tools to boost the efficiency and safety of advanced therapies to cure genetic and oncological diseases with high unmet medical need.

I have a strong scientific background in

... Read More →
avatar for Jon Alberdi

Jon Alberdi

CEO, VIVEbiotech

avatar for Laura Rodríguez Gallego

Laura Rodríguez Gallego

Partner, Invivo Partners

Tuesday September 29, 2026 16:00 - 16:45 CEST
4 Raúl Martín room

16:00 CEST

Women’s health & care as a growing industry
Tuesday September 29, 2026 16:00 - 17:00 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. Another case is that of migraine, an under-recognized women's health problem. Its high prevalence in women, the gender gap in diagnosis, and diagnostic delays have a significant economic, occupational, and social impact impacting career paths, leisure time, social life, and reproductive decisions.

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.

A call to political action: propose a national health plan with a gender perspective, more training in primary care, more sex-disaggregated research, and greater institutional recognition.


Speakers
avatar for María Amparo Valladares López

María Amparo Valladares López

Market Access Value Proposition & Government Affairs Lead, AbbVie

avatar for Eva Colás Ortega

Eva Colás Ortega

CSO & Founder, Mimark
I am the principal investigator of the Biomedical Research Group in Gynecology, where I lead the translational research group. My research focuses on providing solutions to unmet clinical needs in gynecology, primarily in endometrial cancer and endometriosis. We work on biomarker... Read More →
avatar for Marina Pollán

Marina Pollán

Director, Instituto de Salud Carlos III (ISCIII)
Marina Pollán holds a degree in Medicine from the University of Salamanca and is a specialist in Preventive Medicine and Public Health. She also studied at the Johns Hopkins School of Public Health (Baltimore, USA) and the Karolinska Institute (Stockholm, Sweden), and received the... Read More →
AV

Ane Vitoria

Scientific Advisory Board, Qassay Diagnostics/Welleo

avatar for Iván Macía Oliver

Iván Macía Oliver

Director of Digital Health & Biomedical Technologies, Vicomtech
- Vicomtech - Director of Digital Health and Biomedical Technologies (abbreviated Director of Health): This is my main role and the one that pays me. The biggest implication here is that I lead CARAMEL, a Horizon Europe project on Personalized Prevention in Women's Cardiovascular... Read More →
avatar for Carlos Escobar Cervantes

Carlos Escobar Cervantes

Cardiologist and co-founder Cofounder SAMIRA DTx, Hospital 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 →
Tuesday September 29, 2026 16:00 - 17:00 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.




Moderators
avatar for James Cameron

James Cameron

Market Specialist for Cell & Molecular Research, Agilent NLD

Speakers
avatar for Carolina Pola

Carolina Pola

CEO, STAb Therapeutics
Multidisciplinary scientific professional with 12 years of experience in building relationships and communicating with different stakeholders in biomedicine including KOLs, foundations, science policy makers and business around the world. Expertise in identifying translational science... 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 →
avatar for Miguel Angel Campanero

Miguel Angel Campanero

Quality Control Manager, Syngoi Technologies
I am passionate about innovation, emerging technologies, and artificial intelligence, with a strong belief in the critical importance of quality systems in managing the lifecycle of medical products.

With 10 years of experience in quality system management, clinical evaluation, technical documentation development, auditing, and certification of medical and in-vitro diagnostic products, I co-founded A3Z Advanced in 2016, a boutique consulting firm that provides comprehensive support

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

09:30 CEST

Beyond Venture Capital Building Alternative Financing Pathways for Biotech Growth
Wednesday September 30, 2026 09:30 - 10:15 CEST
This round table will explore the growing range of alternative funding instruments available to innovative biotech SMEs, from public equity markets to emerging deeptech investment funds backed by public-private initiatives.
Moderated by Óscar Salazar (Euro-Funding), the discussion will bring together representatives from BME Growth, ICO AXIS, and a listed Spanish biotech company to share practical insights on how different financing options can support sustainable growth at different stages of a company's journey. Panelists will discuss how BME Growth can serve as a strategic financing platform for innovative SMEs, address common misconceptions and concerns surrounding stock market listings, and share first-hand experiences of accessing public markets. The conversation will also examine the role of new deeptech funds in closing financing gaps and complementing traditional investment sources.
Attendees will gain a clearer understanding of how alternative financing mechanisms can expand the capital toolbox available to biotech companies, helping founders and executives make informed decisions as they scale their businesses and navigate an increasingly diverse funding landscape.

Moderators
avatar for Oscar Salazar

Oscar Salazar

Managing Director European Funds, EURO FUNDING
Managing Director en la unidad de Fondos Europeos en Euro-Funding, donde lidera un equipo multidisciplinar de más de 30 profesionales internacionales, incluido el equipo de la oficina de Bruselas. Con casi tres décadas de trayectoria profesional, ha desarrollado una sólida carrera... Read More →
Speakers
avatar for Jesús González Nieto-Márquez

Jesús González Nieto-Márquez

Managing Director, BME Growth & BME Scaleup
Jesús González is the Managing Director of BME GROWTH and BME SCALEUP (the Spanish markets for SMEs), where more than 140 companies are traded, with a market capitalization exceeding €19 billion. He is also the Managing Director of Latibex, the Latin American Stock Exchange in... Read More →
avatar for Mercedes Storch

Mercedes Storch

FondICO Next Tech Director, AXIS Participaciones Empresariales SGEIC
More than 20 years linked to ICO/AXIS in different departments and a global point of view of ICO as development  bank. Currently FondICO Next Tech Investment Management and International Relations. Previously, in capital markets dep, involved in the structuration of ICO´s first... Read More →
avatar for Olatz Azpiazu Aguirre

Olatz Azpiazu Aguirre

Financial Manager, ELKARGI

avatar for Manuel Ramos

Manuel Ramos

CEO, LABIANA LIFE SCIENCES S.A.U.
Seasoned C-Suite Executive with 20 years of experience. My journey started as an Auditor and Consultant and took me to Senior Strategy and Private Banking.  I then moved on to Business Recovery Services in Restructuring and NPLs which took me to my current roles at Labiana where... Read More →
Wednesday September 30, 2026 09:30 - 10:15 CEST
4 Raúl Martín room

09:30 CEST

Biotech Act: Accelerating Biotech Scale-Up and Building Competitive Value Chains in Europe
Wednesday September 30, 2026 09:30 - 10:15 CEST
Following the publication of the proposed Biotech Act I Regulation, the European Commission has launched a consultation process for the future Biotech Act II, which will focus on industrial policy and on building a broad, forward-looking biotechnology ecosystem.In this session, organised by AseBio, we will examine the opportunities presented by Biotech Act II to advance biomanufacturing and biotechnology innovation in Europe, while also addressing the regulatory, financing, and scale-up challenges facing the sector.
Moderators
avatar for Ion Arocena

Ion Arocena

General Manager, AseBio

Speakers
avatar for Ana María Bravo

Ana María Bravo

Director of Public Affairs at IFF and President of Industrial Biotechnology Council Europabio, International Flavors & Fragance (IFF) / Europabio

avatar for Miguel Gómez-Pavón López

Miguel Gómez-Pavón López

Directorate-General for Industrial Strategy and Small and Medium-sized Enterprises (SMEs), Ministry of Industry and Turism
Industrial engineer from the ETSII-UPM with over 15 years of experience in the design and implementation of public policies, financial cooperation, and industrial strategy. My professional career has unfolded at the intersection of industry, innovation, and public action, with a common... Read More →
avatar for Kristin Schreiber

Kristin Schreiber

Director Chemicals, Bioeconomy and Retail, DG GROW.F, European Comission

Wednesday September 30, 2026 09:30 - 10:15 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia

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 proposed panel creates a strong and complementary storyline around the clinical translation of bioprinting technologies:

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
BO

Beatriz Olalde

Director of Healthcare Biomaterials, TECNALIA

Speakers
avatar for Anthony Remazeilles

Anthony Remazeilles

Medical Technology Researcher, TECNALIA
Anthony Remazeilles estudió ingeniería informática en el Institut National des Sciences Appliquées (INSA) en 2001, cuenta a su vez con máster en Informática e Inteligencia Artificial (Universidad de Rennes 1, 2001) y desde 2004 es doctor en ingeniería informática por la Universidad... Read More →
avatar for Begoña Ferrari

Begoña Ferrari

COO & Cofounder, COLFEED4PRINT S.L.
Scientific Researcher of CSIC at the Institute of Ceramic and Glass. She is in charge of R&D operations and the provision of human and economic resources to the team. At the CSIC, she is leading the research on the processing of complex ceramic and metallic composites by colloidal... Read More →
avatar for Francisco Miguel Sánchez Margallo

Francisco Miguel Sánchez Margallo

Scientific Director, 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
Dr. Jesús María Izco Zaratiegui is a prominent Spanish executive and scientist who serves as the Bioproducts Diversification Manager (Director General del Departamento de Diversificación) at Viscofan S.A., a global leader in casings for the food industry. 
Under his leadership... Read More →
LM

Luc Milbergue

President, 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

10:15 CEST

Biomanufacturing at an Inflection Point: Technology Breakthroughs, Scale-Up Challenges and the Future of the CMO Model
Wednesday September 30, 2026 10:15 - 11:00 CEST
This round table brings together perspectives from across the bioprocessing and biomanufacturing value chain. The discussion will explore major technological breakthroughs, including single-use systems, process intensification, automation, continuous bioprocessing, advanced analytics, AI and digitalization, while examining their real-world impact on process development and manufacturing. Speakers from SEDA Manufacturing Development Services, Celltoki, Lonza, Alfa Laval and Agilent will address the challenges of translating innovative processes from development to GMP and commercial scale, including technology transfer, process robustness, data quality, analytical control and manufacturing efficiency. The roundtable will also consider how new equipment, smarter analytics and more sustainable processing technologies can improve productivity and flexibility. A key part of the conversation will focus on the evolving CMO/CDMO business model, including integrated development and manufacturing services, flexible capacity, strategic partnerships and risk-sharing approaches. By bringing together technology providers, process specialists and manufacturing organizations, the session aims to provide a balanced view of the opportunities and bottlenecks shaping the future of biomanufacturing.

SEDA Pharmaceutical Development Services Development-to-manufacturing integration, CMC, manufacturability, clinical supply and flexible outsourced development models

Alfa Laval. Analytical technologies, process understanding, characterization, quality and data-driven manufacturing
Speakers
avatar for Tom Manelius

Tom Manelius

Business Development Single-Use separation, Alfa Laval
I am a business driven engineer with a base in international sales development, marketing and sales support roles. I have also worked in Technology/Business Development, Product Management, Project Management and Consultancy positions. I truly enjouy working where business and technology... Read More →
avatar for Marcel de Matas

Marcel de Matas

Founder & Chief Business Officer, Seda Pharmaceutical Development & Clinical Manufacturing Services
Marcel is Founder and Chief Business Officer at Seda, a company focussed on delivering chemistry manufacturing and controls (CMC) and clinical pharmacology services. The company is located in Cheadle, Stockport and supports companies across UK, Europe, US, Asia and Australia.

Marcel has led the growth of technical capabilities and services at Seda, and has been instrumental in its transformation from a consultancy based business to an internationally recognised contract research, development, and manufacturing organisation. Services include the development

... Read More →
avatar for Natalia Serrano Morillas

Natalia Serrano Morillas

Key Account Manager, Celltoki
Professional with over 10 years of experience in health sciences, including the last 5 years in the biotech industrial sector. I have held roles in project and operations management related to the manufacturing of bioprocess equipment, with key responsibilities in planning, monitoring... Read More →
Wednesday September 30, 2026 10:15 - 11:00 CEST
3 Nicolás Achúcarro room

10:15 CEST

Regulating Intelligence: Bringing AI-Powered Medical Devices to the European Market under MDR and the AI Act
Wednesday September 30, 2026 10:15 - 11:00 CEST
Artificial intelligence is transforming medical devices, particularly software-based technologies for early disease detection and personalised healthcare. However, in 2026 AI-powered medical devices in Europe will operate under a dual regulatory framework shaped by Regulation (EU) 2017/745 (MDR) and the Artificial Intelligence Act, creating one of the most complex compliance environments globally.
This session will bring together a Notified Body representative, a startup with an AI-based speech analysis platform for early detection of dementia, Parkinson’s disease and cardiovascular conditions, and regulatory strategy experts. The panel will provide a multidisciplinary and practice-oriented discussion on how innovative AI solutions can successfully reach the European market.
Key discussion points include:
  • Qualification and classification of AI-based software as medical devices
  • Clinical evidence expectations for machine learning systems
  • Lifecycle management of adaptive algorithms
  • Interaction between MDR and the AI Act requirements
  • Data governance and high-risk AI systems
  • Regulatory pitfalls and common deficiencies identified by Notified Bodies
  • Strategic considerations for startups scaling internationally
The discussion will address whether Europe can maintain global competitiveness in digital health while ensuring patient safety and regulatory robustness. By combining regulatory authority perspective, industry experience and strategic advisory insight, this session offers a practical roadmap for innovators navigating AI medical device development in Europe.
Moderators
avatar for Itziar Alkorta Idiakez

Itziar Alkorta Idiakez

Professor, Euskal Herriko Unibertsitatea

Speakers
OB

Oskar Berreteaga Castro

QA & Compliance Manager, Irisbond Crowdbonding SL
Before my current position, I was CTO at Irisbond, Systems Engineering and Software Development Manager at ULMA Embedded Solutions, and a Researcher at Ikerlan. During my consulting work, I collaborated with several companies that had to comply with international standards including... Read More →
avatar for María Teresa Gómez Manzano

María Teresa Gómez Manzano

Medical Devices Iberia Manager/Medical Devices Lead Auditor, SGS
My professional career began in 2001, at the age of 23, as Quality and Environmental Manager at the multinational company PIMAN, with offices in Alcalá de Henares, Seville, Barcelona, ​​Poland, Morocco, and China, specializing in the metal sector.

Subsequently, in 2002, I joined the consulting firm Alta Calidad Consultores S.L., in the Quality, Environment, and Prevention Department. For the next four years, I held the position of junior consultant and later senior consultant. My responsibilities included providing legal advice... Read More →
avatar for Talyta Carteano

Talyta Carteano

Medical Devices Director., Asphalion
Talyta started at Asphalion as Medical Device Manager and Lead Auditor in 2020, bringing over 10 years’ experience in the Medical Devices field. She combines a technical background with a fulfilling career in the fields of regulatory affairs, quality management systems, devices development and leading people.She has proved to be key to the company since the very beginning thanks to her experience, which covers multiple... Read More →
Wednesday September 30, 2026 10:15 - 11:00 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia

10:15 CEST

Translating Breakthroughs to Next‑Generation Therapies for ALS
Wednesday September 30, 2026 10:15 - 11:00 CEST
Amyotrophic Lateral Sclerosis (ALS) poses 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 ALS. 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 paid to cross-disciplinary collaboration and innovation. 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
  • 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.


Moderators
MS

Maite Solas

Vice-president, FUNDELA

Speakers
avatar for Manuel Cuervas-Mons Cantón

Manuel Cuervas-Mons Cantón

Medical Lead Innovative Medicines, Bristol Myers Squibb (BSM)
Medical Doctor, PhD, and board-certified surgeon with over 10 years of clinical experience in a tertiary hospital, where I led complex surgical cases and coordinated the Foot & Ankle Unit.

Driven by the ambition to improve patient outcomes beyond the operating room, I transitioned

... Read More →
avatar for Yosu Vara

Yosu Vara

Chemistry and Manufacturing Director, cofounder, Quimatriyx
He has 20 years of experience in the biotechnology and pharmaceutical industry, where he has managed drug discovery projects. He is the author of more than 20 patents and publications in organic chemistry.
He holds a PhD in Organic Chemistry from the University of the Basque Count... 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 & Scientific Advisory Board Member, 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 10:15 - 11:00 CEST
2 Dorotea Barnés room

11:30 CEST

Fishing in the Atlantic Marine Biotech Innovation Ecosystem: from potential to societal impact
Wednesday September 30, 2026 11:30 - 12:15 CEST
Fishing in the Atlantic Marine Biotech Innovation Ecosystem: A Comprehensive Examination of Emerging Scientific and Technological Potential, Pathways for Development and Commercialization, Policy and Governance Challenges, and the Tangible Societal Impacts on Coastal Economies, Public Health, Biodiversity Conservation, and Community Resilience This expanded formulation frames a broad, multi-dimensional exploration of the Atlantic marine biotechnology and fisheries landscape — tracing how basic research and nascent technologies move through translational development, entrepreneurship, and regulatory systems into real-world applications. It highlights interconnected topics such as sustainable resource management, value-chain innovation (from bioprospecting to bio-based products), equity and livelihoods for coastal communities, environmental and biodiversity considerations, and measurable benefits to public health, regional economies, and social well-being. The emphasis is on understanding not just the scientific potential but also the institutional, economic, and societal mechanisms that determine whether innovations deliver meaningful, equitable impact.
Moderators
avatar for Elisabete da Costa

Elisabete da Costa

Scientific and Technological Advisor (PhD in Sustainable Chemistry), BLUEBIO ALLIANCE

Speakers
LC

Luís Costa

Chief Scientific and Sustainability Officer, A4F

avatar for Tiago H. Silva

Tiago H. Silva

Principal Researcher. Academic & Research Staff, University of Minho - Biomaterials, Biodegradables and Biomimetics Research Group.
PhD in Chemistry (Analytical Chemistry/Electrochemistry) - Universidade do Porto, 2006
 
Graduation in Chemistry (Analytical Chemistry) - Faculdade de Ciências da Universidade do Porto, 2001
 
Research Area:
MARINE INSPIRED BIOMATERIALS: Marine origin polymers and ceramics in Tissue Engineering; Valorization of marine resources and by-products; extraction/isolation and characterization of marine polymers (chitosan, collagen, fucoidan) and ceramics (calcium phosphates and biosilica); development... Read More →
avatar for Marta Conde Sieira

Marta Conde Sieira

Professor, Universidade de Vigo - Marine Research Center
Prof. Marta Conde-Sieira has developed her career in aquaculture, specializing in fish physiology, stress, and appetite regulation. After earning her PhD at the University of Vigo, she conducted postdoctoral research in Portugal, focusing on Senegalese sole and sustainable aquafeeds... Read More →
avatar for Ibon Cancio

Ibon Cancio

Full Professor, University of the Basque Country
Associate Professor in Cell Biology in UPV/EHU, accredited for Full Professorship by Spanish ANECA in May 2010 (positive answer of University for promotion July 2020). He has been coordinator of the official Masters degree in “Environmental Contamination & Toxicology” from 2012... Read More →
Wednesday September 30, 2026 11:30 - 12:15 CEST
3 Nicolás Achúcarro 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 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

David Blanco

Managing Director, Leanbio

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

11:30 CEST

The Role of Regional Ecosystems in Driving the Biotech Sector
Wednesday September 30, 2026 11:30 - 12:15 CEST
Regional biotechnology clusters and associations play a vital role in strengthening the biotechnology ecosystem by promoting collaboration among stakeholders, facilitating knowledge transfer, and accelerating the scientific and business development of the sector. Their work enhances the competitiveness of biotechnology companies while reinforcing the innovation and growth potential of their respective regions.

The aim of this session is to examine the role of biotechnology clusters and bioregions in the development of the sector, explore how they collaborate with one another, and identify the key strengths and challenges across different regions, highlighting both shared priorities and the distinctive characteristics of each regional ecosystem. The discussion will also address the Biotech Act proposal to promote networks of biotechnology clusters as a means of strengthening competitiveness and fostering collaboration across the European biotechnology sector.
Speakers
avatar for Carlota Gómez de la Hoz

Carlota Gómez de la Hoz

Chief Corporate Affairs & Sustainability Officer, LABORATORIOS HIPRA S.A.

DA

Daniel Álvarez

International Development Manager, Bioga

ZP

Zara Pons Vila

Managing Director Biotechnological and Biomedical Cluster of the Balearic Islands – Gerent/Gerente, BIOIB - Clúster Biotecnològic i Biomèdic de les Illes Balears

avatar for Idoia Muñoz Lizán

Idoia Muñoz Lizán

Managing Director, Basque Health Cluster (BHC)

avatar for Robert Fabregat

Robert Fabregat

CEO, BIOCAT
Robert Fabregat (Barcelona, 1980) holds a degree in Chemistry and a PhD in Pharmacy from the University of Barcelona (UB), as well as a Master’s degree in Project Management from BES-La Salle and specific training in Strategy and Innovation from ESADE. From 2019 to 2021, he was... Read More →
avatar for Jesús Agüero González

Jesús Agüero González

Director, BIOVAL
I am a biologist with a PhD, and my research background includes a thesis in biotechnology. Using molecular biology tools, genetic engineering, and microscopy, we used a citrus virus to study its movement within the plant and introduced the instructions for it to express small pr... Read More →
Wednesday September 30, 2026 11:30 - 12:15 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia

12:15 CEST

Can Cooperative Models Transform the Future of Pharma and Healthcare?
Wednesday September 30, 2026 12:15 - 13:00 CEST
What would it take to make cooperative enterprises viable at scale in the life sciences ecosystem? How can these models attract investment while preserving their core values? And could they unlock more resilient, inclusive, and patient-centered innovation systems? This roundtable will bring together leaders from healthcare, industry, policy, and cooperative movements to explore the opportunities and limitations of rethinking enterprise models in pharma and beyond.
 
Participantes propuestos
  • Representante de RPK (si hubiera opción, pendiente de confirmación)
  • Representante de una institución vasca (si hubiera opción, pendiente de confirmación)
Speakers
avatar for Raúl Pérez

Raúl Pérez

Scientific Director, I+Med.

avatar for Manuel Sánchez-Lagarejo

Manuel Sánchez-Lagarejo

General Manager, 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

12:15 CEST

From Lab to Market: Financing Spain’s Deep-Tech Future through Innvierte & Tech Transfer and the EIC Accelerator
Wednesday September 30, 2026 12:15 - 13:00 CEST

Spain is doubling down on early-stage innovation with the launch of the Innvierte Deep-Tech & Tech Transfer programme, led by CDTI Innovación under the Ministry of Science, Innovation and Universities (MICIU), in collaboration with the European Investment Fund. With a total allocation of €353 million targeting early-stage technologies (TRL 2–4), the initiative aims to address Spain’s critical funding gap between research and commercialization—unlocking the potential of universities, research centers, and spin-offs.
This round table will explore how public-private co-investment models—such as the recent €30 million commitment to the Montana Children’s Health Fund, managed by Ship2B Ventures—can help catalyze a stronger deep-tech ecosystem. Bringing together perspectives from public investors, fund managers, and the European Investment Bank’s EIC Accelerator programme, the discussion will examine how institutional capital and blended financing can de-risk early innovation, strengthen technology transfer, and help breakthrough science reach the market.
Panelists will discuss the key challenges facing deep-tech ventures in Spain, from bridging the gap between research and investability to accessing the right mix of grants, equity, and institutional capital. The conversation will also explore how European-level instruments such as the EIC Accelerator can complement national initiatives and provide a pathway for high-potential companies to scale beyond their domestic markets.
Key questions include: How can Spain better align financial instruments with the needs of deep-tech entrepreneurs? What lessons can be drawn from the first Innvierte transaction? How can national and European funding mechanisms work together more effectively? And how can investors, corporates, universities, and public actors collaborate to accelerate the journey from lab to market and build globally competitive companies?
The session is designed for investors, fund managers, technology transfer offices, policymakers, corporates, and entrepreneurs seeking to understand and engage with Spain’s evolving deep-tech financing landscape—and the opportunities emerging at the intersection of national and European capital.

Moderators
avatar for Ángel Sánchez

Ángel Sánchez

Partner, Science & Innovation Link Office (SILO)

Speakers
avatar for Myriam Rouis

Myriam Rouis

Senior Investment Manager/Advisor, EIC Fund - Venture Capital

avatar for Moisés Martín Carretero

Moisés Martín Carretero

General Director, CDTI

José Moisés Martín Carretero university degree in economics from the Universidad autónoma de Madrid and has extended graduate programs in finance from the IE Business School, Economic Analysis in the national and international economic relations in the CEPADE from Universidad... Read More →
avatar for Marc Ramis Castellfort

Marc Ramis Castellfort

Founder & Managing Partner, Montana
Marc is passionate about building ventures in the life sciences. He is co-Founder and Managing Partner of the Montana Children’s Health, a venture capital fund managed by Ship2B Ventures, where he focuses on creating and scaling companies dedicated to children’s health and pediatric... Read More →
avatar for Clara Campás

Clara Campás

Managing partner and co-founder of Asabys, Asabys Partners
Managing partner and co-founder of Asabys. Clara currently serves on the board of directors of Ona Therapeutics, Nuage Therapeutics, ALLOX and Augustine Therapeutics.Formerly, Clara served as Strategy & Development Director at Kern Pharma and held several positions at Advancell, including... Read More →
Wednesday September 30, 2026 12:15 - 13:00 CEST
4 Raúl Martín room

12:15 CEST

From Science to Market: The Value of Engineering Across the Biotech Product Lifecycle
Wednesday September 30, 2026 12:15 - 13:00 CEST
How early technical choices sculpt scalability, manufacturability, regulatory success and market readiness. Engineering doesn’t wait for shovels in the ground. It begins the moment a scientist chooses a route in the lab — a decision that can ripple through industrial design, regulatory strategy and the economic fate of a product. This roundtable will celebrate engineering as a continuous creative force across the entire biotech journey — from initial discovery and process development, through industrialization and GMP manufacture, to commercialization. 
 
The goal is to show engineering not as a finishing touch but as a guiding hand that helps teams make smarter choices at every turn. 

1) The role of engineering throughout the product lifecycle Think of engineering as the cartographer, bridge-builder and translator of the development path. When engaged early, it helps teams to: - Anticipate technical risks before they become crises. - Design for scalability so a lab success can grow into a reliable plant process. - Reduce regulatory uncertainty by embedding compliance-minded choices into the workflow. - Smooth technology transfer so knowledge travels cleanly from bench to plant. - Shape industrialization strategies that align process design with real-world constraints. - Strengthen investor confidence by turning technical stories into credible execution plans. - Accelerate time-to-market by avoiding late-stage rework and surprises. At heart, many seemingly late-stage failures trace back to early experimental choices. When engineering is part of those choices, the pathway to market becomes clearer and more navigable. 

2) Crossing the “valleys of death” The development journey is punctuated by perilous transitions — from research to process development, from process development to GMP manufacture, from manufacturing readiness to investor readiness, and from regulatory approval to commercial traction. These so-called “valleys of death” swallow promising innovations when technical, regulatory and economic realities are not anticipated. Introducing engineering thinking early is like building bridges and laying maps across those valleys: it reduces surprises, shortens detours and raises the odds that a promising technology will reach patients and markets.
Moderators
avatar for Jordi Gibert Amat

Jordi Gibert Amat

Head of Biotechnology Unit, KLINEA
Experienced engineer with a demonstrated history of working in the Biotechnological and Pharmaceutical industry. Skilled in  R&D, innovation management, bioprocessing, process scale-up, process industrialization and GMP production.
Wednesday September 30, 2026 12:15 - 13:00 CEST
2 Dorotea Barnés room

12:15 CEST

New Approach Methodologies (NAMs): Accelerating Safer, Smarter and More Human-Relevant Innovation in Drug and Chemical Development
Wednesday September 30, 2026 12:15 - 13:00 CEST
New Approach Methodologies (NAMs) are transforming the way drugs, medical products, and chemicals are evaluated by providing more predictive, human-relevant, and sustainable alternatives to traditional testing approaches. By integrating advanced in vitro models, computational tools, artificial intelligence, in silico toxicology, and innovative preclinical strategies, NAMs offer new opportunities to improve safety assessment, reduce development timelines, lower costs, and support regulatory decision-making.
This round table will bring together leading experts from industry and technology providers to explore the current state and future potential of NAMs across the life sciences sector. The discussion will examine how emerging methodologies are being implemented in research and development workflows, the scientific and regulatory challenges that remain, and the collaborative efforts needed to accelerate adoption.
Representatives from CMG MedDev, ProtoQSAR, Labcorp and IVT Becytes will share their perspectives on the role of digital technologies, predictive modeling, advanced biological systems, and regulatory science in shaping the next generation of safety and efficacy assessment.
The session will address key questions including:
  • How can NAMs improve the predictivity and translational value of preclinical testing?
  • What role do AI, computational toxicology, and in silico approaches play in modern risk assessment?
  • How are regulators responding to the growing adoption of NAMs?
  • What barriers are limiting broader implementation, and how can they be overcome?
  • How can collaboration between biotechnology companies, technology developers, regulators, and investors accelerate the transition toward human-relevant innovation?
Attendees will gain practical insights into the opportunities and challenges associated with NAMs, as well as a forward-looking view of how these technologies are reshaping drug development, chemical safety assessment, and the broader bioeconomy.


Moderators
avatar for Carmen Martín González

Carmen Martín González

CEO & Founder, CMG Meddev SL

Speakers
avatar for Natalia Sánchez

Natalia Sánchez

Senior Scientific Advisor, BeCytes Biotechnologies (BioIVT)

avatar for John Kendrick

John Kendrick

Executive Director, NAMs and Emerging Technologies, Labcorp
Over the past 20 years, I have worked diligently to build and refine my skills in Drug Development, with a particular focus on the scientific elements that make up DMPK. I have continued learning and evolving the skills for scientific and organizational leadership of this discipline... Read More →
avatar for Simón Perera del Rosario

Simón Perera del Rosario

Business Development Manager, ProtoQSAR
Simón. Simón Perera holds a degree in Biotechnology from the Autonomous University of Barcelona and a Master's degree in Biological Anthropology from the University of Barcelona.

He has worked as a project manager and business developer at various companies, including Anaxomics... Read More →
Wednesday September 30, 2026 12:15 - 13:00 CEST
3 Nicolás Achúcarro room

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.


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.
Moderators
avatar for Pedro Carrascal

Pedro Carrascal

General Director, Platform of Patient Organisations
I have been involved with the multiple sclerosis movement since I was 8 years old, when my mother was diagnosed with MS. At that time, she and others founded the Bizkaia Association. I served as director of ADEMBI (Bizkaia Multiple Sclerosis Association) for 25 years (until 2022... Read More →
Speakers
avatar for Tabikh Ammar

Tabikh Ammar

Senior Medical Director, Clinical Development Global Medical Lead - Medical Strategy -Nephrology, CTI Clinical Trial & Consulting
As a Physician and Senior Medical Director in Clinical Development, I bring extensive experience leading global clinical programs across nephrology, transplantation, rare diseases, immunology, and metabolic disorders. Throughout my career, I have collaborated with sponsors, CROs... Read More →
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 →
Wednesday September 30, 2026 14:30 - 15:15 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia

14:30 CEST

Unlocking Opportunities in precision fermentation for the food industry
Wednesday September 30, 2026 14:30 - 15:15 CEST
Imagine a kitchen where tiny, tireless chefs—yeast, bacteria, or fungi—are taught new recipes at the molecular level. That is precision fermentation: a carefully controlled, biology-driven process that programs microorganisms to churn out specific food ingredients, from enzymes and flavor molecules to structurally complex proteins. Using modern genetic and metabolic engineering, these microbial artisans produce high-purity molecules that once came only from animals or cumbersome extraction processes, offering a platform that’s predictable, scalable, and potentially kinder to the planet.

One of the clearest and most evocative examples of this approach is the creation of recombinant caseins. Caseins—the alpha, beta and kappa family members that give milk its character—are the architect proteins that assemble into micelles, creating milk’s texture, emulsifying power, and its ability to be turned into curds for cheese.

That said, the path from fermenter to supermarket shelf has practical hurdles: regulatory approval pathways, production economics, downstream processing and quality control, supply-chain integration, and consumer acceptance all matter. Overcoming these requires engineering, rigorous testing, smart economics, and clear communication about safety and benefits.
Speakers
JL

Jose Luis Moreno Carboneros

Business Development & Application Manager, COCOON

avatar for Laura Pedrós Manzanares

Laura Pedrós Manzanares

Business Developer, Levprot Bioscience

avatar for Guadalupe Monserrat Alvarado Jasso

Guadalupe Monserrat Alvarado Jasso

Researcher in culinary biotechnology, Basque Culinary Center/GOe Tech Center
I am a highly accomplished and strategic-minded professional with a Ph.D and a scientific approach to in managing research, development, and innovation projects, with extensive experience in leading multidisciplinary teams and optimizing resources. My scientific and strategic approach... Read More →
avatar for Ana Torrejón Cabello

Ana Torrejón Cabello

Head of Microbiology and Industrial Biotechnology, AINIA
Chemical Engineer (Polytechnic University of Valencia, 2006) and Master in Agri-food Biotechnology (University of Valencia, 2019).She is currently the Head of Microbiology and Industrial Biotechnology at AINIA. She has over ten years of experience in scaling up biotechnological processes... Read More →
Wednesday September 30, 2026 14:30 - 15:15 CEST
3 Nicolás Achúcarro room

15:15 CEST

Circularity at Scale: The 2030 Value Chain Challenge
Wednesday September 30, 2026 15:15 - 16:00 CEST
The European Union has positioned the bioeconomy as a cornerstone of its competitiveness, sustainability, and strategic autonomy agenda. The recently launched Strategy for a Competitive and Sustainable EU Bioeconomy seeks to accelerate the transition from innovation to industrial deployment by removing regulatory barriers, scaling investment, creating lead markets for bio-based solutions, and strengthening sustainable biomass value chains.

This roundtable will explore how Europe's new policy framework can translate into growth opportunities for biotechnology companies, investors, industrial partners, and regional innovation ecosystems. Discussions will focus on the practical implications of the strategy's four pillars: accelerating innovation and scale-up, developing markets for bio-based products and technologies, securing sustainable feedstocks and circular value chains, and strengthening Europe's global leadership in the bioeconomy.

Bringing together representatives from industry, policymakers, investors, and innovation organizations, the session will examine the actions needed to move bio-based innovations from the laboratory to commercial deployment. Particular attention will be given to regulatory modernization, industrial financing, public procurement, advanced biomanufacturing, and the creation of demand for sustainable bio-based solutions.

As Europe seeks to build resilient value chains and reduce dependence on fossil-based resources, this discussion will highlight how biotechnology can become a key driver of industrial transformation, economic growth, and environmental sustainability across the continent.

Key discussion questions:
  • How can Europe accelerate the scale-up and commercialization of bio-based innovations?
  • What regulatory and financing mechanisms are needed to strengthen industrial biotechnology competitiveness?
  • How can lead markets be created for bio-based materials, chemicals, food ingredients, and advanced biomanufacturing solutions?
  • What role should public procurement and industrial partnerships play in driving demand?
  • How can Europe strengthen its strategic autonomy while ensuring sustainable and circular biomass value chains?
This framing aligns much more closely with the European Commission's 2025 Bioeconomy Strategy and AseBio's advocacy around regulatory streamlining, industrial scale-up, investment mobilization, and market creation.

Ya he contactado con estos y estos pendiente de su contestación, excepto ASINCAR que ya ha dado el ok.
  • Celignis, Irlanda, SME, Agrifood
  • Decathlon, Francia, Industria, Textil
  • Novamont, Italia, Industria, Bioplasticos


Moderators
avatar for Lara Valentín

Lara Valentín

Senior Innovation Consultant & Team Leader Circular Bioeconomy, PNO Innovation
I transform ideas into real and profitable innovation projects. I have been working in research and innovation for 20 years. The first 10 years my research was about contaminants and technologies to treat polluted sites. Since 2014 I have been dedicated to management and development... Read More →
Speakers
avatar for Armando Menéndez Estrada

Armando Menéndez Estrada

R&D&I Project Manager, ASINCAR

avatar for David San Martín Errea

David San Martín Errea

Senior Researcher, AZTI
Bachelor of Science in Biology from the University of Santiago de Compostela (USC); Advanced Technician in Aquaculture Production from the Institute of Agricultural and Fisheries Research and Training (IGA.FA); and Advanced Technician in Occupational Risk Prevention from Juritecn... Read More →
Wednesday September 30, 2026 15:15 - 16:00 CEST
3 Nicolás Achúcarro room

15:15 CEST

Current innovation trends in therapeutic technologies and modalities: what is the potential of Spain to ride these waves?
Wednesday September 30, 2026 15:15 - 16:00 CEST
Mapping where the next therapeutic breakthroughs are emerging in Spain—key institutions, technologies and talent—and how to access and translate them into investment and company-building opportunities.

A guided tour of Spain’s biomedical frontier: where tomorrow’s therapies are being born, who’s driving them, which technologies enable them, and how to convert those breakthroughs into investment and company-building opportunities
Moderators
avatar for Montserrat Vendrell

Montserrat Vendrell

Partner, Asabys Partners
Montse currently serves on the board of directors of Ona Therapeutics, InBrain Neuroelectronics, Peptomyc and Accure. She is also independent director at the board of Oryzon genomics.Formerly, Montse was partner at Aliath Bioventures and Alta Life Sciences. Prior to that, she was... Read More →
Speakers
avatar for Gloria González

Gloria González

Researcher / CSO, CIMA / Amets Biotechnology
She holds a degree in Biology from the University of the Basque Country. She earned her PhD from the Autonomous University of Madrid after completing her doctoral thesis at the Center for Biological Research (CBI) of the Spanish National Research Council (CSIC) in Madrid, under the... Read More →
avatar for Pilar Carrato

Pilar Carrato

Director of finance and innovation, CDTI
She began her professional career as a financial analyst at the Bank of Spain.

Subsequently, she developed her financial career in various securities and stock exchange firms in their international departments for 12 years, eventually becoming Head of Sales and Trading at BCH and... Read More →
avatar for Robert Fabregat

Robert Fabregat

CEO, BIOCAT
Robert Fabregat (Barcelona, 1980) holds a degree in Chemistry and a PhD in Pharmacy from the University of Barcelona (UB), as well as a Master’s degree in Project Management from BES-La Salle and specific training in Strategy and Innovation from ESADE. From 2019 to 2021, he was... Read More →
avatar for Gurutz Linazasoro

Gurutz Linazasoro

Founder, VIVEbiotech
Gurutz es neurólogo especializado en enfermedad de Parkinson y trastornos neurodegenerativos. Es Director del Programa de Terapias Avanzadas para el Alzheimer y Parkinson del Grupo Quirón Salud-Policlínica Gipuzkoa, y Director del Curso Nacional Anual sobre Trastornos del Movimiento.Gurutz... Read More →
Wednesday September 30, 2026 15:15 - 16:00 CEST
2 Dorotea Barnés room

15:15 CEST

Substance Matters: From Microbiome Breakthroughs to EU Benchmarks
Wednesday September 30, 2026 15:15 - 16:00 CEST
Human-derived substances are at the forefront of a new wave of biomedical innovation, spanning cell therapies, microbiome-based interventions, and advanced medicinal products. As these technologies rapidly evolve, so too does the complexity of the regulatory landscape governing their development and clinical application within the European Union.
This session will explore the scientific, clinical, and regulatory dimensions of substances of human origin (SoHO), with a focus on how emerging frameworks aim to balance patient safety, ethical considerations, and innovation. Experts will provide insights into the latest EU regulatory developments, including classification challenges, compliance pathways, and the implications of the evolving SoHO regulation.
A featured perspective from industry will highlight real-world translation, showcasing how cutting-edge companies—such as those working in microbiome therapeutics—navigate regulatory uncertainty while advancing novel therapies toward the clinic. The discussion will emphasize practical strategies for stakeholders across biotech, healthcare, and policy to effectively bring human-derived innovations to market.
Join us to unpack what truly constitutes “substance” in today’s biotech ecosystem—and how Europe is shaping its future.

Speakers
avatar for Claudio Hidalgo Cantabrana

Claudio Hidalgo Cantabrana

CEO, Microviable Therapeutics
Co-founder and CEO at Microviable Therapeutics. Claudio obtained his PhD at the University of Oviedo (2015) focused on microbial genetics, probiotics and microbiome, after MS Biotechnology and BS Biology. Claudio has worked in several research international organizations across Europe... Read More →
avatar for María José Reyes

María José Reyes

Regional Regulatory Regional Director Europe, Clarke y Modet
At Clarke Modet my focus as Regulatory Consulting Director Europe is provide to our customers with Regulatory and Quality strategies and solutions for medicines and Medical devices to distribute pharmaceutical and Medical devices. With an extensive background in regulatory affairs... Read More →
avatar for Dominika Misztela

Dominika Misztela

Director Global Regulatory Science, Policy, and Intelligence Europe, CSL Behring
Highly motivated, ambitious, and skilled multilingual professional with demonstrated expertise in regulatory affairs and clinical project management and across EU and non-EU countries. 

Excellent knowledge of European research structures and frameworks and extensive regulatory ex

... Read More →
avatar for Patricia del Río

Patricia del Río

Executive Director, Mikrobiomik
Con más de tres años de trayectoria en Mikrobiomik, Patricia ha sido una pieza clave en su crecimiento, comenzando como Responsable de Ensayos Clínicos y más recientemente como Directora de Desarrollo de Negocios e Innovación.
Antes de unirse a Mikrobiomik, Patricia lider... Read More →
Wednesday September 30, 2026 15:15 - 16:00 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia

16:00 CEST

One Health Diagnostics: Rapid Detection and Characterization of Multidrug Resistant Bacteria to Enable Next Generation Antimicrobials
Wednesday September 30, 2026 16:00 - 16:45 CEST
Imagine a crossroads where human health, animal welfare, and the environment meet — and a new generation of sentinels stands guard. This panel will convene those sentinels to tackle the urgent challenge of protecting vulnerable people and animals from disease driven by major antibiotic‑resistant threats, and to showcase the bleeding‑edge tools that spot and dissect multidrug‑resistant bacteria across clinical, food and environmental landscapes within a One Health framework. We’ll voyage through the knotted realities of vaccine development and market access, then move into the fast‑moving world of diagnostics: gene‑based LAMP assays that turn hours into minutes, electrochemical biosensors that read microbial whispers as electrical signals, nanomaterial‑amplified methods that reveal the faintest traces of pathogens, microfluidic “lab on a chip” platforms that miniaturize whole laboratories, and point‑of‑care systems built for real‑world decisions. The growing appreciation for vaccines—from immune surrogates of protection to fresh insights into host‑pathogen dynamics and sharper disease definitions—will be explored as a keystone for prevention. Recent breakthroughs already sound like science fiction: sub‑hour detection of key AMR genes, ultra‑low limits of detection in messy samples, and real‑time antimicrobial susceptibility testing that brings clinical and research timelines into alignment. These advances not only sharpen bedside decision making but also feed drug discovery with high‑resolution pathogen profiles that accelerate new antimicrobial development. The panel will bring together thought leaders in vaccines, diagnostics, microfluidics, biosensing, environmental microbiology, and pharmaceutical innovation to chart the next frontiers in AMR detection — and to imagine how those frontiers will reshape the hunt for tomorrow’s drugs.

Introduction – The One Health Challenge of MDR Bacteria

Block 1 - From Immunity to Impact: Building Executable AMR Vaccines
Block 2 – Genetic Detection of MDR Bacteria: LAMP and Other Rapid Molecular Techniques
Block 3 – Electrochemical Biosensing: Fast, Sensitive Characterization of MDR Bacteria
Block 4 – Point of Care Devices and Lab on a Chip Systems for Rapid AMR Decision-Making
Block 5 - Connecting Diagnostics to Drug Developement: TheFeedback Loop

Looking ahead to 2035, what single technological or ecosystem change would have the greatest impact on transforming AMR detection from a reactive activity into a predictive and actionable One Health system?

Moderators
avatar for Raquel Carnero

Raquel Carnero

Senior Medical Devices Specialist, IQVIA

Speakers
avatar for Juan José Infante Viñolo

Juan José Infante Viñolo

CEO, Vaxdyn
Dr. Infante leads Vaxdyn and its international collaboration network, advancing vaccines against antibiotic-resistant bacteria. As co-inventor of the company's core technology, he has secured funding from CARB-X, the European Commission and specialist investors. His background combines... Read More →
avatar for Larraitz Añorga Gómez

Larraitz Añorga Gómez

Director of Research and Development, Biolan Health SL
R&D Director with a strong scientific background and more than 15 years of experience leading R&D&i projects focused on the design, development, and manufacturing of (bio)sensors (lateral flow immunoassays, electrochemical biosensors based on printing technologies, etc.) for food... Read More →
avatar for Santos Merino

Santos Merino

Senior Researcher & Surface Chemistry and Nanotechnology Unit, TEKNIKER

PhD in Solid State Physics in 1997. Since 2001, he was Head of the Micro and Nanofabrication Unit in IK4-Tekniker and since 2017 he is Head of the Sensors Research Area in the Surface Chemistry and Nanotechnologies Unit. He has worked on different fields such as in-vitro diagnostic tra... Read More →
avatar for Bruno González-Zorn

Bruno González-Zorn

Head of Antimicrobial Resistance Unit and Prof at UCM, Universidad Complutense de Madrid (UCM)
Bruno González Zorn, is a prominent microbiologist, scientist, and professor. He is recognized for his pioneering contributions to One Health and antimicrobial resistance (AMR). His work has had a significant impact on the global understanding of zoonotic diseases and the development... Read More →
Wednesday September 30, 2026 16:00 - 16:45 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia

16:30 CEST

MythBusters: The Realities of Biotech Capital
Wednesday September 30, 2026 16:30 - 17:15 CEST
Speakers
avatar for Avencia Sánchez Mejías

Avencia Sánchez Mejías

CEO & Co-founder, Integra Therapeutics
Proud to be leading Integra Therapeutics, a biotech company that is creating next-generation gene writing tools to boost the efficiency and safety of advanced therapies to cure genetic and oncological diseases with high unmet medical need.

I have a strong scientific background in

... Read More →
avatar for Malgorzata Rogalska

Malgorzata Rogalska

Analyst, Ysios Capital

Wednesday September 30, 2026 16:30 - 17:15 CEST
4 Raúl Martín 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.


Moderators
avatar for Carmen Martín González

Carmen Martín González

CEO & Founder, CMG Meddev SL

Speakers
avatar for María Teresa Gómez Manzano

María Teresa Gómez Manzano

Medical Devices Iberia Manager/Medical Devices Lead Auditor, SGS
My professional career began in 2001, at the age of 23, as Quality and Environmental Manager at the multinational company PIMAN, with offices in Alcalá de Henares, Seville, Barcelona, ​​Poland, Morocco, and China, specializing in the metal sector.

Subsequently, in 2002, I joined the consulting firm Alta Calidad Consultores S.L., in the Quality, Environment, and Prevention Department. For the next four years, I held the position of junior consultant and later senior consultant. My responsibilities included providing legal advice... Read More →
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

16:45 CEST

Rare Diseases at a Turning Point: From Gene Editing to Precision Medicines
Wednesday September 30, 2026 16:45 - 17:30 CEST
Rare disease research is entering a transformative era. Advances in precision medicine, in vivo gene editing and novel therapeutic modalities are opening unprecedented opportunities to address conditions that have long lacked effective treatments. However, scientific innovation alone is not sufficient. Translating breakthrough discoveries into accessible therapies requires overcoming significant challenges in clinical development, manufacturing, regulation and healthcare implementation.
This round table will explore the opportunities and barriers shaping the next generation of rare disease therapies, with particular attention to ophthalmology and central nervous system (CNS) disorders. Experts from biotechnology, pharmaceutical industry and translational research will discuss how emerging technologies—including in vivo gene editing and other precision therapeutic approaches—are changing treatment paradigms, while examining practical issues such as innovative clinical trial designs for ultra-rare populations, scalability of development programmes, biomarker-driven patient selection, and the path towards sustainable access.
The discussion will highlight how collaboration between academia, biotech, industry and healthcare systems can accelerate the delivery of innovative therapies to patients, positioning Spain and Europe as key contributors to the future of rare disease innovation.

Potential speakers

  • Biobizkaia/Bioaraba
Speakers
avatar for Óscar Millet

Óscar Millet

Group Leader Precision Medicine and Metabolism Lab, Atlas Molecular Pharma
I hold a Bachelor's degree in Chemistry (Ramon Llull University, 1994) and a Bachelor's degree in Chemical Engineering (IQS, 1995). After obtaining a PhD in Organic Chemistry (University of Barcelona, ​​1999), I joined Lewis Kay's group in Toronto for a postdoctoral fellowship... Read More →
avatar for María Fernández Jiménez

María Fernández Jiménez

Value, Access & Policy Director, AMGEN

avatar for Inmaculada Gilaberte Asin

Inmaculada Gilaberte Asin

Global Head Clinical Research Department, FAES Farma
PERSONAL PROFILE
o    Growth Mindset
o    Prioritize patients’ needs in every aspect of clinical strategy and execution.
o    Lead with a diverse, team-oriented collaborative approach, fostering strong collaboration across global multidisciplinary teams
o    Deliver results



... Read More →
avatar for Amalia Capilla

Amalia Capilla

CEO, Miramoon Pharma
Dr. Amalia Capilla is CEO of Miramoon Pharma and a biotech executive with 20+ years of experience in regenerative medicine, gene and cell therapy, and translational research. She holds a PhD in Molecular Biology from the University of Valencia and completed postdoctoral training at... Read More →
Wednesday September 30, 2026 16:45 - 17:30 CEST
2 Dorotea Barnés room
 
Thursday, October 1
 

09:30 CEST

From Lab Coats to Suits: Essential Roles in the Biotech Journey
Thursday October 1, 2026 09:30 - 10:15 CEST
· Moderación: Persona 
· Ponentes:
o Perfil I+D: David Álvarez Ordás (Roche)
o Perfil Manufacturing / Operations: Persona de 3P BIOVAN
o Perfil Regulatory Affairs: Persona de Viralgen
o Perfil Marketing: Persona de HIPRA

Thursday October 1, 2026 09:30 - 10:15 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia

10:15 CEST

Magnetize & Maintain: Speeding up attraction, securing long-term retention
Thursday October 1, 2026 10:15 - 11:00 CEST
Mesa redonda 2: “Magnetize & Maintain: Speeding up attraction, securing long-term retention”
· Moderación: Persona de FEBiotec
· Ponentes:
o Perfil consultoría HR: Persona de otra consultora
o Perfil STEM: Persona de Bizkaia Talent
o Perfil formación: Persona de CESIF
o Perfil HR en empresa biotec: Paola Salanueva (Histocell)

Thursday October 1, 2026 10:15 - 11:00 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia

11:30 CEST

Unlocking the Lab: Navigating Patents and the Spin-off Landscape
Thursday October 1, 2026 11:30 - 12:15 CEST
· Moderación: Persona de FEBiotec
· Ponentes:
o Perfil patentes: Persona de Manuel Illescas
o Perfil inversor: Persona de Ysios Capital


Speakers
CI

Cristian Izquierdo

International Group Recruiter, PNO INNOVATION

avatar for Malgorzata Rogalska

Malgorzata Rogalska

Analyst, Ysios Capital

avatar for Teresa Riesgo Alcaide

Teresa Riesgo Alcaide

Secretary General for Innovation, Minstry of Science, Innovation and Universities
Professor of Electronic Technology at the Higher Technical School of Industrial Engineers of the UPM (ETSII-UPM), where she has developed her entire teaching and research career.Professional experienceShe has been director of the Center for Industrial Electronics, deputy director of Research and International Relations of the ETSII-UPM and, more recently, director of the Department of Automation, Electrical Engineering and Electronics and Industrial Informatics.Since 2003 she has... Read More →
avatar for Jascha Blobel

Jascha Blobel

Founder & Chief Executive Officer, Golden Gait Biotech
Jascha Blobel is working since over 15 years in the development of biotech companies. Has has been involved in 3 out-licensing deals. As co-founder and CEO of Molomics Biotech, the company was sold to San Fransisco based VeriSIM Life in 2022. Jascha studied chemistry at the Ludwig-Maximilians... Read More →
Thursday October 1, 2026 11:30 - 12:15 CEST
1 Margarita Salas auditorium Azkue Kalea, 1, 48902 San Vicente de Barakaldo, Bizkaia

12:15 CEST

Job Opportunties of the Future: AI and the Digital Transformation of Biotech".
Thursday October 1, 2026 12:15 - 13:00 CEST
Moderación: Persona de una spin-off no elegida como ponenteo Perfil spin-off: BioComputing o HAWK Biosystems / Ubikare
o Perfil automatización: Persona de Agilent technologies
o Perfil uso IA para búsqueda fármacos: Persona de MSD
o Perfil uso IA en CDMO: Persona de Klinea

Speakers
LM

Lourdes Martínez Martínez

Director of Career Services, CESIF

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