What gene therapy vectors do you support?

We provide end-to-end CDMO support for AAV and other viral vectors, including process development, analytics, GMP manufacturing, and QC.

Do you offer process characterization and QC analytics?

Yes. We run DoE-driven process characterization with platform assays and comprehensive QC analytics aligned to regulatory expectations.

Can you support tech transfer and scale-up?

We manage tech transfer from development through scale-up with stage-appropriate comparability and documentation for efficient GMP readiness.

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Pharmaron is a leading Cell and Gene Therapy CDMO, delivering comprehensive cell and gene therapy development services from our state-of-the-art cGMP biomanufacturing facility in Liverpool, UK. As a trusted CGT CDMO, we offer advanced analytical platforms, high-throughput process development, and purpose-designed viral and plasmid GMP manufacturing suites to support your cell and gene therapy projects.