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4basebio

Synthetic DNA and RNA CDMO for next-generation genetic medicines, from research to clinical production.

4basebio manufactures high-quality synthetic DNA and RNA using proprietary cell-free amplification technology, supporting mRNA vaccines, viral vectors, gene editing, and cell/gene therapies from research through GMP-grade clinical production. Headquartered in Over, United Kingdom.

Modalities

Development & manufacturing

Structured CDMO capabilities from verified public sources.

Biologics / bioreactor infrastructure

Expression systems
Cell-Free

Regulatory clearances

Services

About this organization

Overview

4basebio is a specialist CDMO providing synthetic DNA and RNA manufacturing services for next-generation genetic medicines. The company operates a GMP-licensed manufacturing facility near Cambridge, UK, and a dedicated enzyme manufacturing facility in Madrid, Spain.

Core Capabilities

Synthetic DNA Manufacturing:

  • Cell-free DNA amplification technology as an alternative to plasmid DNA (pDNA)
  • Available in RUO, HQ, and GMP-grade formats
  • opDNA® for mRNA vaccines and therapeutics
  • hpDNA for viral vector production and DNA vaccines
  • ssDNA for gene editing applications
  • Eliminates bacterial sequences, host-cell contaminants, and antibiotic resistance genes
  • 4x faster production compared to pDNA with enhanced purity

RNA Services:

  • mRNA manufacturing derived from synthetic DNA templates
  • saRNA manufacturing
  • Comprehensive manufacturing services with precise control over each development stage

Formulation & Delivery:

  • Hermes® nanoparticle platform for DNA and RNA delivery
  • LNP formulation services enabling continuous link between DNA template production, RNA synthesis, and encapsulation

Applications Supported

  • mRNA vaccines and therapeutics
  • Viral vector manufacturing (AAV and other vectors)
  • Gene editing platforms
  • DNA vaccines
  • Personalized cancer therapies
  • Non-viral delivery systems
  • Cell and gene therapies

Regulatory & Quality

  • GMP-licensed manufacturing facility at Buckingway Business Park, Swavesey, Cambridge
  • Purpose-built cleanrooms and advanced quality control systems
  • In-house enzyme manufacturing ensures supply chain control and consistency
  • Regulatory expertise in process development and compliance
  • Demonstrated FDA IND approval support (Tier 1 pharma partner mRNA product in Phase I/II clinical trial as of October 2025)

Manufacturing Scale

Capabilities span from early-stage research-grade production through full-scale GMP manufacturing, with dedicated support teams worldwide for process development, regulatory compliance, and project management.

Certifications

AuthorityIdentifierSource
UK GMPGMP-licensedView

Locations

  • Headquarters and R&D

    Over · Cambridge · United Kingdom

  • GMP Manufacturing Facility

    Swavesey · Cambridge · United Kingdom

  • Enzyme Manufacturing Facility

    Madrid · Madrid · Spain

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