hVIVO Solutions Overview

hVIVO delivers integrated solutions supporting life science innovators across all stages of drug development, from early design to clinical execution. Whether end-to-end or targeted support, our model ensures seamless coordination. Scientific leaders, experienced project managers, and specialist teams drive efficient delivery, bringing deep expertise across clinical pharmacology, infectious disease, respiratory, and cardiometabolic research.

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Clinical Pharmacology

hVIVO accelerates development via Phase I clinics, human challenge models, biometrics, medical monitoring, and Phase II/III sites across UK & Germany.

Human Challenge Trials

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.

Laboratory

Providing highly specialised infectious disease and immunology laboratory services, hVIVO is an expert in immunology, molecular, and cell-based assay development, with advanced sample handling and testing using the latest platforms to support sponsor requirements from pre-clinical to Phase III.

Drug Development Consultancy

Together with sponsors, we shape efficient, milestone‑driven development programmes that move science forward. With broad therapeutic expertise -, we help teams reduce uncertainty, refine programme strategy and reach the clinic faster, with certainty.

Integrated Solutions

hVIVO delivers fully integrated solutions that support life science innovators across every stage of drug development—from early programme design to clinical execution. Whether a comprehensive, end‑to‑end pathway or targeted support such as operational delivery, site services, or recruitment, our model brings seamless coordination.

Storage

hVIVO provides end‑to‑end biobanking and sample storage solutions. Whether you require long‑term preservation, short‑term project storage, or an integrated partner to handle sample intake, processing, monitoring and retrieval, our infrastructure supports the full lifecycle of clinical and research samples.

Full-Service
Early Phase CRO

hVIVO is a full-service early phase CRO offering end-to-end drug development services from preclinical consultancy through to Phase III clinical trials, including world leading end-to-end human challenge trials services. With decades of experience in rapidly delivering data for our global client base, our team brings together strategic insight and operational expertise to deliver a variety of clinical study types across multiple locations.

To support rapid study start-up and reliable delivery, our dedicated recruitment teams in Germany and the UK provide direct access to both healthy volunteers and patient populations. This is complemented by our integrated drug development consultancy as well as our infectious disease and immunology laboratories and biobanking services.

100+

Years of Service, Reputation & Trust

Over a century of combined experience in clinical research and infectious disease. Our heritage underpins the expertise and credibility we bring to every study.

Key Areas of Expertise

Integrated capabilities across consultancy, clinical trials, laboratories, human challenge studies, and recruitment. Together, these services provide a seamless end-to-end development platform.

400k

Trial Participants Database

Access to one of the largest specialist volunteer databases in Europe. This enables rapid recruitment and high retention to keep studies on track.

1.9k

Trials Completed & Counting

A proven track record of successfully delivering a high volume of clinical trials across multiple phases and therapeutic areas. We focus on quality, efficiency, and reliable outcomes.

Clinical Sites

A network of purpose-built clinical research facilities across the UK and Germany. Designed to support efficient trial delivery, including complex and early-phase studies.

Discover hVIVOs Integrated Solutions

Speed-to-Clinic

Speed-To-Clinic Accelerator

Critical path analysis to accelerate development start up

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Investor Readiness

Investor Readiness Consulting: Prioritise activities and evidence investors value to unlock Seed/Series A/B or acquisition

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Clinical Trial Delivery

Full-service integrated solution across the drug development pathway, prior to IND enabling, through Phases I and II combining our consultancy, laboratory and clinical offerings to deliver end-to-end services

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Translational

Translational Consulting Research

Bridge R&D to clinic with GLP/GCP-ready methods and operational execution

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Human Challenge

Human Challenge Advantage

Competitive advantage. Use proven challenge trials to generate early efficacy signals and accelerate PoC 3.5 faster than non challenge

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EU Strategy

EU Strategy

Agile support to expand study delivery in to Europe

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Site & Recruitment

Site and Recruitment Solutions

Qualified sites, specialist populations & expedited

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Sectors we service

We partner with start-ups, biotech, pharmaceutical companies, and CROs to deliver flexible, high-quality clinical solutions tailored to each stage of development. By combining clinical operations, recruitment, and specialist laboratory services, we simplify complexity, accelerate timelines, and generate robust data to support confident decision-making across diverse clinical programs.

Start-Ups