
Oxford Biomedica
30 years of viral vector expertise. End-to-end CDMO solutions for cell and gene therapies.
Global viral vector CDMO with 30 years of expertise in lentivirus, AAV, and adenovirus manufacturing. Provides end-to-end development and GMP-compliant manufacturing services from preclinical through commercial launch for cell and gene therapy programs. Headquartered in Oxford, United Kingdom.
Modalities
Development & manufacturing
Structured CDMO capabilities from verified public sources.
Development (D)
Manufacturing (M)
Biologics / bioreactor infrastructure
- Expression systems
- MammalianCell-FreeViral Vector
- Bioreactor type
- Single-Use / DisposableStainless Steel
- Max bioreactor scale
- Mid-scale clinical (≤2,000 L)
Fill-finish formats
Regulatory clearances
Services
- Process Development
- CMC Analytical Development
- Viral Vector Manufacturing
- Lentiviral Vector Manufacturing
- AAV Manufacturing
- Vaccine Manufacturing
- Sterile Fill-Finish & Aseptic Manufacturing
- Upstream Processing
- Downstream Processing
- Technology Transfer
- CMC Regulatory Submission Support
- Cell Therapy Manufacturing
Indications
About this organization
Overview
Oxford Biomedica (OXB) is a global, full-service, quality and innovation-led viral vector CDMO specializing in the development, scale-up, and GMP-compliant manufacture of cell and gene therapy products. Founded in 1995 as a spin-out from the University of Oxford, OXB has evolved into a leading contract development and manufacturing organization with over 30 years of experience in viral vector technology.
Core Capabilities
Viral Vector Platforms:
- Lentivirus: 30 years of pioneering experience; scalable production from 50L to 1000L across harmonized global processes
- AAV: Proprietary inAAVate™ platform delivering GMP AAV in as little as 7 months; achieves titres of 1.5E+17vgs from 500L bioreactors with 90% full capsids
- Adenovirus: Proven large-scale manufacturing (100+ million doses of Oxford–AstraZeneca COVID-19 vaccine); flexible end-to-end CDMO model
- Other vectors: MVA (Modified Vaccinia Ankara) and other poxvirus-based vectors for immuno-oncology and infectious disease vaccines
Service Models:
- Platform projects for preclinical/early-clinical clients seeking accelerated GMP timelines with proven processes
- Custom solutions offering flexibility for preclinical/early-clinical development
- Technology transfer for Phase I, II, and III programs requiring scale-up and long-term manufacturing
Regulatory & Infrastructure:
- End-to-end regulatory support from preclinical development through commercial launch
- Multiple IND and MAA submissions supported
- FDA Drug Master File (DMF) maintained
- GMP facilities in UK, Europe (France), and USA
- State-of-the-art infrastructure aligned to global regulatory standards
Market Position
Recognized by Fortune as one of Europe's Most Innovative Companies in 2025. Trusted partner to leading biopharma companies, biotech firms, and start-ups worldwide.
Certifications
| Authority | Identifier | Source |
|---|---|---|
| FDA | Drug Master File (DMF) | View |
Locations
Facility
UK · United Kingdom
Facility
Europe · France
Facility
USA · United States
Headquarters
Oxford · Oxfordshire · United Kingdom
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Oxford · Oxfordshire · United Kingdom
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Oxford · Oxfordshire · United Kingdom
Wallingford Manufacturing
Wallingford · Oxfordshire · United Kingdom
Yarnton Manufacturing
Oxford · Oxfordshire · United Kingdom
Bedford Manufacturing
Bedford · Massachusetts · United States
Durham Manufacturing
Durham · North Carolina · United States
Lyon Manufacturing
Lyon · Auvergne-Rhône-Alpes · France
Strasbourg Manufacturing
Illkirch-Graffenstaden · Grand Est · France
EU Support Office
Dublin · Dublin · Ireland
Chancery Gate Manufacturing
Oxford · Oxfordshire · United Kingdom
Yarnton Manufacturing
Yarnton · Oxfordshire · United Kingdom
US Facility
United States · United States
European Facility
France · France
Recent news about Oxford Biomedica
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