Confirmed Exhibitors

3p Biovian

ABG Intellectual Property

ABG Intellectual Property (ABG IP, previously named ABG Patentes) has been for the last 22 years one of the most important references in Europe when talking about IP services, having the largest team of patent and trademark attorneys in Spain (Madrid, Barcelona, Bilbao and Valencia):
23 European Patent Attorneys (all qualified through examination EQE)
10 Spanish Patent & Trademark Agents
4 Attorneys-at-Law
22 Ph.D.s in diverse areas of technology
5 UPC Representatives
The firm totals thirty-nine professionals with exclusive dedication, and a complete team of almost eighty people including experienced paralegals and support staff.
ABG IP advises clients ranging from individual investors, small companies and startups, universities and research institutions to big multinational corporations on patents, trademarks, designs and associated aspects of intellectual property.
Our team brings a fresh approach to IP. We work in close contact with our clients and understand their technology and fields of activity. We provide solid, valuable advice to our clients taking their needs and strategic goals into account.
ABG is known for:
- Its expertise in all technical fields. The firm’s attorneys are highly regarded for their in-depth technical knowledge, understanding of the science behind patented inventions as well as practical backgrounds. They are entrusted with cases in the most complex areas of patent law and technology;
- A deep knowledge of the European patent system, counting with 2 former EPO examiners;
- A deep knowledge of the Spanish, European and International Trademark system, counting with a former EUIPO examiner;
- Extensive experience in both Spanish and European patent, trademark and design prosecution, patent litigation proceedings and IP strategy;
- Recognized expertise in Supplementary Protection Certificates (SPC) prosecution.
- Handling of worldwide trademark portfolios including clearance searches;
- Our trademarks team is particularly strong in the defense of well-known trademarks and in the management of oppositions before the Spanish Patent and Trademark Office (SPTMO) and the European Union Intellectual Property Office (EUIPO).
- The high-quality legal and litigation services provided as a consequence of the optimization of the existing synergies in the IP field between our experienced Attorneys-at-Law and patent and trademark attorneys.
- A leading role on the implementation of trade secrets protection programs.
- A solid competence in plant variety protection.
- We are also a reference firm for the training of highly competitive IP professionals.

Abioinnova

Albian

Aseptic Group

The ASEPTIC GROUP is specialised in aseptic fluid transfers. An independent pioneer in single-use systems dedicated to bioproduction, we are the specialist in sterile fluid transfer solutions in critical environments.

Our 2 complementary activities make us an experienced partner that is recognised in the market, notably:
- Proven expertise for more than 20 years in marketing single-use components suited to a wide range of applications
- The design and production of custom single-use assemblies, ready for use in ISO Class 7 in activity clean room

Our total independence enables us to guarantee you the right solution for your needs.

Our markets are pharmaceutical and biotechnology industries, and main applications are:
- Vaccines
- Injectable drugs
- Cell & Gene therapies

Our main customers are the majors within those industries.

Our ready-to-use single-use assemblies allow you to:
- optimise your prodution processes
- get your products to market faster
- simplify and streamline your supplies
- reduce your costs

For more information, feel free to visit us:
www.aseptic-group.com

Asphalion

ASPHALION is an international Regulatory, Scientific & Safety consultancy company with offices in Barcelona, Madrid, Munich, London, and Pamplona. Since its foundation in 2000, ASPHALION has grown consistently to employ over 190 professionals representing more than 16 nationalities. Its strong track record has established ASPHALION as a key player in the international healthcare sector and a major contributor to the implementation of new regulatory standards.
ASPHALION provides expert consulting, strategic advice, operational support, and full outsourcing services for all product life cycle stages across all therapeutic areas. Its team offers tailored solutions for Pharmaceutical, Biotechnological, and Medical Technology companies, having successfully delivered over 5,000 projects for more than 1,000 clients from over 50 countries. Services span non-clinical and clinical development, CMC, dossier writing, regulatory procedures, vigilance, eSubmissions, and data management for both medicinal products and medical devices.
The company’s expertise is particularly notable in the field of Advanced Therapy Medicinal Products (ATMPs), where their team possesses specialized scientific knowledge and extensive regulatory experience. ATMPs require unique development strategies and regulatory adaptations due to their complexity. ASPHALION provides comprehensive support, including drafting regulatory, non-clinical, clinical, and CMC documentation essential for development, registration, and lifecycle management. Additionally, they offer strategic guidance on segmentation, niche indications, conditional approvals, fast-track processes, orphan drug designations, and preclinical and clinical development plans to minimize time-to-market.
ASPHALION has been a leader in ATMP regulatory support since 2005, participating in over 30 projects covering cell therapy (autologous and allogenic derived stem cells, CAR-T) and gene therapy (oncolytic viruses, adeno-associated virus (AAV), Modified Vaccinia Virus (MVA), Plasmids, Lentivirus, Adenovirus (AdV), and more). By collaborating closely with international competent authorities, notified bodies, scientific associations, and key opinion leaders, ASPHALION ensures the delivery of optimal solutions for every project. Their comprehensive network of geographic and functional partners further solidifies their ability to meet the needs of a dynamic and evolving healthcare landscape.

Cencora

Our full-service logistics and storage solutions help you seamlessly deliver innovation.
We manage the logistics for your most precious innovations. And we don’t take that responsibility lightly. Across our global network of dedicated team members, we monitor the safety and integrity of your product proactively, ensuring it reaches patients without delay. We plan for contingencies, so you don’t have to, leveraging our global capabilities and local, on-the-ground knowledge to navigate logistics complexities. Our innovative distribution services for medications, including rare, orphan, and gene therapies, are customized and scalable to fit your product’s needs.

We go the extra mile to ensure increased supply chain efficiency, maximum return on investment, and enhanced patient care.

Biocat

Charles River

Charles River is a leading global CRO supporting biotech and pharmaceutical companies across the entire early drug‑development continuum. We provide research models, discovery and safety assessment services, and manufacturing and biologics testing solutions, enabling clients to accelerate preclinical research and advance therapies toward the clinic.

Charles River has supported work on over 80% of FDA‑approved drugs in the past five years and offers an integrated portfolio spanning in vitro and in vivo studies, toxicology, pharmacology, cell and gene therapy support, and microbial testing. With operations in 20+ countries and recognized expertise built since its founding in 1947, we serve as a critical partner helping biotech innovators de‑risk and streamline the development of novel therapeutics.

CMG MedDeV

CMG MedDev es un socio estratégico en regulación, calidad y desarrollo clínico para empresas y startups innovadoras en biotech y tecnología médica. Apoyamos su crecimiento con estrategia regulatoria , marcado CE, FDA y generación de evidencia clínica, de forma eficiente y segura para acceso un acceso al mercado más rápido.

¿Desarrollas un producto innovador en salud o salud digital?
En CMG MedDev te ayudamos a definir la estrategia regulatoria y clínica para Europa y EEUU iy te llevamos hasta el marcado CE y FDA, validación y generación de evidencia maximizando el valor de tu proyecto.

MDR / IVDR / MDSW / MD-AI

¿Hablamos?

Curapath

Curapath is a CDMO specializing in novel drug delivery systems (DDS) with expertise in LNP and PNP formulation and GMP manufacturing. We support the entire therapeutic journey, from development to Commercial, providing GMP manufacturing for Drug Substance and Drug Product. With unmatched technical and analytical expertise, we design, develop, and manufacture polymer- and lipid-based DDS for cell therapy, gene therapy, and vaccines. For over a decade, we’ve supported innovators with excipients, polymers, and linkers, accelerating drug development with hands-on guidance and scalable solutions

EHU

Innoprot

Innoprot is a biotechnology company with a primary focus on advancing cell-based assays and technologies tailored for drug discovery. Our technological platforms include Nomad Biosensors, crucial for multiplexing G Protein-Coupled Receptor (GPCR) screening assays. We have also developed in vitro models that accurately replicate cellular pathways associated with major neurodegenerative diseases, such as Parkinson's Disease, Alzheimer's Disease, and Amyotrophic Lateral Sclerosis. Additionally, we offer fibrosis assays designed for use across a broad range of primary and immortalized cell lines.

Our cell lines are well-suited for translational research involving 2D and 3D models, organ-on-a-chip technology, and microfluidic devices. Innoprot is dedicated to advancing drug discovery through state-of-the-art technologies and versatile cell-based solutions

IVACE

IVACE is a public body depending on the Regional Ministry of Innovation, Industry, Commerce and Tourism from the Region of Valencia. In IVACE Internacional we support companies on their paths to internationalisation. Thanks to our broad network of delegations in 35 markets we can offer tailored services to help the companies find distribution channels abroad and we are also experts in organising international fairs and trade missions to foster their worldwide relationships. Among all the exporting sectors in the Region of Valencia, biotechnology stands out as one of the most dynamic and competitive, and IVACE International works also in fostering their international presence.

Jori Armengol

JORI& – Strategic Risk & Insurance Consulting Since 1890

JORI& is an independent insurance brokerage and risk consulting firm founded in 1890, with a long-standing tradition of advising companies through complex and evolving risk environments.

We specialize in providing tailored insurance and risk management solutions to innovative and high-growth sectors, including Life Sciences, Biotechnology, MedTech, Digital Health, and DeepTech.

Our approach goes beyond traditional insurance placement. We work as strategic partners to founders, CEOs, CFOs, and boards, helping them identify, assess, and transfer critical risks across every stage of growth — from early R&D and clinical trials to international expansion and scaling.

Our expertise includes:

Clinical Trials Insurance (local & multinational programs)

Product Liability & Professional Liability

Directors & Officers (D&O) coverage

Cyber Risk & Data Protection

Intellectual Property risk solutions

Property & Operational risk programs

International insurance structuring

As active partners within innovation ecosystems, we collaborate with research institutions, biotech hubs, investors, and industry associations to support sustainable and secure growth.

At JORI&, we believe insurance is not just protection — it is a strategic tool that enables innovation, investment, and long-term progress.

You make your decisions. We secure your progress.

We look forward to connecting with fellow innovators at BioSpain 2026.

Klinea

Klinea especializada en ingeniería de procesos para la industria Biotech y Farma, ofreciendo soluciones sólidas y a medida. Destaca por su liderazgo en optimización de la producción bajo normativas GMP y FDA, y por impulsar la digitalización con auditorías y planes estratégicos. Integra la sostenibilidad como pilar clave, desarrollando soluciones eficientes y responsables para el futuro del sector.

Leitat

Leanbio

Leanbio is a cutting-edge CDMO specializing in bioconjugation and complex biologics, including recombinant proteins, antibodies, and mRNA. With both microbial and mammalian production platforms, Leanbio delivers seamless, end-to-end biopharmaceutical development and GMP manufacturing services.

The company provides tailored cell line and process development solutions, supporting programs from standard monoclonal antibodies to complex and novel biologics, including ADCs.

Litek Pharma

Litek Pharma es una empresa especializada en el diseño y la fabricación de equipos tecnológicos avanzados para el procesamiento aséptico y aséptico-tóxico.

Nos centramos en la producción de aisladores y RABS personalizados para operaciones de Fill&Finish a pequeña escala y liofilización, así como en soluciones para la producción de terapias avanzadas, test de esterilidad y contención de productos de alta potencia, cumpliendo con los más altos estándares de seguridad.

Ofrecemos soluciones de test de guantes y de RTP tester para ensayos de integridad de guantes y de contenedores de transferencia alfa y beta, al igual que sistemas de transferencia de materiales con o sin VHP.

Molefy Pharma

Neural Omega

Neural Omega is a biotechnology company at the intersection of proteomics, AI, and patient care. We operate two interconnected verticals: Neural Omega Research, developing in silico discovery and protein analysis tools for scientists and clinicians; and Neural Omega Health, building intelligent platforms for the global autoimmune community. Our mission is to make the inherent complexity of molecular biology intuitive and actionable; for the researchers advancing human knowledge and the millions living with autoimmune conditions worldwide. Based in Madrid, we are building the infrastructure for a new era of collaborative, accessible science.

PNO Innovation

PNO Innovation is a leading European innovation and funding consultancy with more than 40 years of experience supporting organisations in turning ideas into meaningful impact. We help organisations navigate the full innovation cycle, from strategy and project development to funding acquisition and implementation, connecting innovation to sustainable growth and societal progress.

With offices across Europe and a multidisciplinary team of experts, we combine deep sector knowledge, financial expertise and an extensive international network to accelerate innovation and maximise success. Driven by people, purpose and impact, we support over 100,000 innovative organisations in addressing today’s major challenges and shaping tomorrow’s solutions.

Quick STAT

For 44 years, QuickSTAT has been providing the leading pharma and biotech companies 24/7/365 global life science logistics solutions from R&D, clinical trials through to commercialization.
Our logistics experts provide time-and temperature-sensitive transport of clinical research samples, cell and gene therapies, investigational drugs, clinical trial supplies and vaccines, to bring new drugs to market. Strict chain of custody, chain of identity and GDP protocols ensure product integrity and patient safety for all clinical and commercial personalized medicines QuickSTAT transports. Consultation and procurement of proper packaging—from controlled room temperature to cryo-frozen. Next-gen IT logistics software provided for managing your clinical supply chain with real-time temperature and tracking technology.

SID

Tekniker

Applied R&D Centre. Our mission is to deliver growth and wellbeing to society at large via R&D&I.

Development and improvement of new/existing medical devices (MDR, IVDR, IA, etc.) and platforms (data space, AI act, etc.) for the detection, monitoring and diagnosis of new diseases, biomarkers, physiological parameters, etc. for more personalised and effective healthcare.

From concept prototypes to market products. ISO 13485 certified.

Market Expertise:

• Smart Medical Devices (MDR)
• Smart in vitro diagnostics (IVDR)
• Medical Robotics
• Imaging diagnosis support systems
• Advanced digital health and connected care
• Reliable artificial intelligence
• Data spaces and interoperable platforms
• Nuclear physics with medical application

Versa Biomedical

VERSA BIOMEDICAL is a pioneering Biomedical Research Centre (CRO) specialized in the pig and cadavers as a preclinical model. We breed our own SPECIPIG® miniature pigs, which are either supplied to external research centres or used in in-house in vivo studies. Projects can also be conducted with other miniature or conventional pigs, depending on the study needs.

Our expertise includes a wide range of preclinical studies:

• Medical devices: Prototype evaluation, biocompatibility, local/systemic tolerance, efficacy, and product development support (ISO 10993).

• Pharmaceutical development (drugs, biomaterials, stem cells, and regenerative medicine): Proof of concept, efficacy, pharmacokinetics, toxicology, and tolerance studies.

• Disease models: Custom-developed or translated from other species. Examples include macular degeneration, NEC in preterm piglets, skin wounds, vascular thrombus, sepsis, swallowing disorders, and myocardial infarction.

• Specialized areas: Dermatology, ophthalmology, cardiology, dental surgery, kidney transplantation, and neonatal/preterm ICU care.

• Human cadaver studies: With real size testing of Medical Devices

• Showroom, demos, surgeon training: With fully equipped ORs.

Studies are conducted in two fully equipped surgical suites and animal housing facilities, supporting both short- and long-term studies (from one day to over two years). VERSA BIOMEDICAL is GLP, ISO 13485 and ISO 9001 certified, follows CE regulations, and has experience with CE and FDA-submitted projects.

Our mission is to deliver tailored solutions and full support across all project stages—from study design and authorization to execution and final reporting.

Wuxi AppTec

WuXi AppTec is a trusted partner and contributor to the pharmaceutical and life sciences industries, providing R&D and manufacturing services that help advance healthcare innovation. With operations across Asia, Europe, and North America, we offer integrated, end-to-end services through our unique CRDMO (Contract Research, Development, and Manufacturing Organization) platform. We are privileged to work alongside partners across 30+ countries, supporting their efforts to bring breakthrough treatments to patients. Guided by our vision that every drug can be made and every disease can be treated, we are committed to advancing breakthroughs for patients—one collaboration at a time.

Zendal

CZ Vaccines belongs to the ZENDAL biopharmaceutical group, which brings together various companies focused on the research, development, manufacturing, and marketing of high value-added biological and pharmaceutical products in the healthcare industry, for both human and animal health.

Our human and animal CDMO services are now unified under the ZENDAL name, so you can find us under the name ZENDAL rather than CZ Vaccines, to better focus on our CDMO services https://www.zendal.com/

ZENDAL is an ideal partner for any organization wishing to advance the development of its biological product candidates, from the development phase to clinical phases I to III, and commercial supply capacity.

We have cutting-edge technology, with solid technical, development, and manufacturing capabilities in VACCINES and THERAPEUTICS.

ZENDAL also contributed to the urgent development of solutions against COVID-19 through our research and manufacturing capabilities.

Your partner for BIOLOGICS manufacturing:

• Live & Inactivated Bacteria & Viral Vaccines up to BSL-2

• Sterile processing systems

• Process Development / Optimisation (Upstream / Downstream)

• Scale-up and cGMP manufacturing

• Aseptic filling into vials

• Lyophilization (clinical trial material and large scale)

• Quality control testing: Microbiological: Sterility-non-sterility, Chemical-Physical and Biological

• Labeling & packaging

• DS & DP release

• Storage: (+2-8ºC), (-30ºC), (-80ºC)

ZBM Patents & Trademarks

ZBM is a firm based on quality and transparency founded at the end of 2003 with the clear objective of helping to change the patent landscape in Spain. More than two decades later, ZBM is proud to have contributed to setting a new standard of quality in patent practice. With this same objective in mind, ZBM staff regularly participate in academic activities to help improve the quality of patent and trademark practitioners in Spain, including those working in other patent firms.
ZBM specialises in the biomedical field, with a completely wide-field view of the sector, our experts having extensive cross-cutting competencies. We work on everything from identifying inventions and protecting them in the broadest possible way, including patents, trade secrets and copyright, following through to conducting freedom-to-operate studies and providing support in any technology transfer process. This comprehensive knowledge of the sector has allowed us to approach venture capital firms, and we regularly carry out due diligence for them in relation to their potential investments.
In short, we are not only familiar with the patent system, but also with the biomedical field itself, including issues such as investment and regulation, this allows us to offer the best personalised service to our clients.