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World Vaccine Congress EU 2026

19-21 October, RAI Convention Centre, Amsterdam

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Meet hVIVO at World Vaccine Congress EU in Amsterdam

hVIVO is proud to attend World Vaccine Congress Europe 2026, the region's leading meeting for vaccine science, development, manufacturing, and partnering. Bringing together stakeholders from across the vaccine value chain, the congress serves as a key forum for sharing scientific advances and exploring new opportunities for collaboration.

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Leading Infectious Disease Research

hVIVO provides unparalleled scientific capability in respiratory infectious disease research, underpinned by decades of virology expertise and a comprehensive suite of validated Human Challenge Models across influenza, RSV, hMPV, HRV, COVID19 and other priority pathogens. Supported by BSL2 and BSL3 facilities, inhouse model development, manufacturing and integrated early phase clinical and laboratory operations, our platform enables precise characterisation of host–pathogen dynamics and high resolution evaluation of novel vaccines and therapeutics. 

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World leader in Human Challenge Trials

World leader in Human Challenge Trials with models for influenza, RSV, hMPV, HRV, COVID‑19, Influenza, and Malaria
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State‑of‑the‑art Human Challenge Unit

State‑of‑the‑art Human Challenge Unit facility with Containment Level 3 (BSL‑3) and onsite BSL‑3 labs.  

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Multiple Pathogen Capability

Expanded capabilities beyond respiratory diseases to pathogens including Dengue, Zika, Norovirus, and Bordetella pertussis
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Over 80+ Human Challenge Studies delivered

Over 80+ Human Challenge Studies delivered, including the first SARS‑CoV‑2 challenge study, and the only commercially available fully characterised models for hMPV, RSV-B and Omicron
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Human Challenge Expertise

Human challenge trials provide a highly controlled and scientifically rigorous environment to evaluate the early efficacy of vaccines, antivirals, monoclonals, and immunomodulators. By exposing healthy adult participants to a well‑characterised viral or bacterial strain in a controlled setting, these studies deliver precise, early readouts that de‑risk development and accelerate decision‑making. hVIVO’s validated challenge models, integrated clinical and laboratory capabilities, and rapid data turnaround enable sponsors to reach proof‑of‑concept up to 3.5× faster than traditional outpatient trials. 

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Challenge Study Models  

Proven to accelerate PoC up to 3.5× faster.

80+

Studies

Controlled viral/bacterial exposure for precise efficacy measurement

5000+

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Integrated clinical and laboratory environment enabling rapid hand off for data analysis and decision making

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Bed Human Challenge Unit

End‑to‑end challenge model design, delivery, and interpretation

Our Services

Clinical

hVIVO supports the full journey from preclinical to Phase III, transforming early Phase I data into clear direction for your product’s next steps. We enable fast success — or fast, informed failure — so you can make smarter decisions sooner.

Our integrated expertise includes:

  • Rapid delivery of safety data & insights through FiH/SAD/MAD/DDI studies in our clinical pharmacology unit combined with our biometry consultancy

  • Accelerate the PoC & efficacy data for your vaccine or anti-viral leveraging our globally recognised Human Challenge Trials using our world-class quarantine facility

  • Expert-led design, rapid recruitment and advanced diagnostic capabilities delivered through our sites in UK and Germany to advance your Phase II/III studies

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Challenge

Building on decades of unrivalled experience, hVIVO is a leading CRO with world-class expertise in delivering human challenge trials, challenge agent manufacture, a unique portfolio of infectious and respiratory disease models, and specialist drug development and clinical consultancy services.

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Labs

hVIVO has a highly specialised infectious disease and immunology laboratory offering a suite of services to support pre-clinical and drug and vaccine discovery & development. 

hVIVO have extended their storage offering to the biotech and pharmaceutical industries with locations in London and Cambridge, offering a dedicated GxP storage facility for biological and clinical materials in secure temperature-controlled conditions.

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Consulting

hVIVO's integrated drug development consultancy supports life science innovators from early planning through clinical execution. With more than 25-years of experience, our team delivers a uniquely combined offering across CMC, non-clinical, clinical pharmacology, regulatory, data management and (translational) laboratory services, across the drug development and market authorisation spectrum.

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Our Attendees

Yasmina-Sahraoui
Yasmina Sahraoui

Vice President & Deputy Head of Business Development

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Alex Mann

Senior Director Clinical Science

Mark Bee
Mark Bee

VP, Business Development

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Simon Kool

Business Development Lead

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Chris Forsdyke

Head of Laboratory Services

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Matthew Blow

Director, Business Development

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Erik Gout

Director, Sr. Consultant CMC

Request a meeting with our team

Content Links

eBook: Advancing Infectious Disease Therapy Development

Blog: Real‑World RSV Maternal Vaccine Data Marks a Turning Point for Infant Protection

Video: Disease characteristics & immunological profiles obtained from hVIVO's hMPV human challenge model

Video: Rethinking clinical research: The case for human challenge trials