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All Viral Vector Services

End-to-End Viral Vector Development and Manufacturing

Minaris delivers end-to-end viral vector solutions designed to accelerate the development of advanced therapies.

With deep expertise across AAV, lentivirus, retrovirus, adenovirus, and other vector platforms, our global team applies proprietary production technologies to achieve higher yields, greater purity, and reliable scalability. From early-stage molecular discovery through process development and cGMP manufacturing at up to 2,000L scale, we provide a seamless pathway to global commercialization.

Our Viral Vector Capabilities

  • Plasmid Engineering

    Plasmid Engineering

    Optimize your payload productivity from the start to mitigate risk and maximize success. Minaris’ SnapFast™ modular plasmids are versatile and efficient. These modular plasmids are designed to work like ‘molecular building blocks,’ using a catalogue of well-characterized DNA elements that can be easily and reliably inserted into specific locations within the plasmid to generate large numbers of custom constructs across a range of expression platforms.

    Our optimized AAV and Lentiviral packaging plasmids are available off-the-shelf to boost yield and accelerate timeline.

  • Cell Banking

    Cell Banking

    Master Cell Bank (MCB) and Working Cell Bank (WCB) are the foundation of biologics
    manufacturing. The quality of these banks determines future manufacturing performance,
    impacting product safety, stability and regulatory compliance. At Minaris, we generate, expand
    and test GMP cell banks for various cell lines, supported by full viral safety testing, release and
    long-term storage.

  • TESSA® AAV 
Production Technology

    TESSA® AAV 
Production Technology

    AAV supply has long been constrained by high costs, low yields, and scalability challenges. Minaris’ proprietary TESSA® technology changes that equation. Delivering 10–50x higher AAV vector productivity than conventional triple plasmid transfection, TESSA® enables cost saving (>90%) per dose and large-scale manufacturing without compromising quality. The platform has been validated across multiple serotypes—including AAV1, AAV2, AAV4–AAV9, AAVrh8, AAVrh10 and AAVrh74—with ranging from up to 50-80% full capsids in crude harvest.

    Our TESSA® technology is fully integrated with in-house testing capabilities, including biosafety assessments, viral clearance, and product release testing. By combining higher titers with superior quality, TESSA® offers a proven path to meeting the market’s growing demand for reliable clinical and commercial AAV supply.

  • XOFLX™ Lentiviral 
Packaging & Producer
Cell Lines

    XOFLX™ Lentiviral 
Packaging & Producer
Cell Lines

    XOFLX™ packaging and producer cell lines stably express genes needed for LVV production, eliminating the need and expense of multiple plasmids. The system utilizes an integrated Tet-inducible VSV-G and Gag-Pol expression strategy and is engineered for low homology between expression cassettes for an improved safety profile. The XOFLX™ cell line was selected for high growth and viability, low aggregation and high productivity. Its robust scalability and low complexity process results in decreased batch-to-batch variation.

  • Cell Line Development

    Cell Line Development

    At Minaris, we support innovators by developing and optimizing robust producer cell lines tailored to program needs. Our integrated services span vector design and construction, clone selection, stability testing and tech transfer. With the right producer cell line strategy, advanced therapy developers can unlock scalable, cost-effective production while maintaining the quality and safety demanded by regulators and patients. Minaris brings the scientific rigor and manufacturing experience to make that possible.

  • Viral Vector Process
Development

    Viral Vector Process
Development

    At Minaris, our experts have established robust platform processes for both AAV and LVV, ensuring yield and purity that meet stringent program requirements. We leverage AMBR15/250 alongside 2-200L bioreactors to move seamlessly from design-of-experiment (DoE) studies through pilot-scale production. With integrated features, Minaris provides a flexible pathway for viral vector process development, optimizing production, scaling up processes, reducing risks, and accelerating timelines.

  • Viral Vector GMP Manufacturing

    Viral Vector GMP Manufacturing

    Minaris delivers clinical and commercial GMP manufacturing of viral vectors from US-based facilities designed for scale and flexibility. Our state-of-the-art suites support adherent processes up to 60-Hyperstacks and suspension culture from 50L to 2,000L. Built with scalability in mind, we leverage single-use technologies, close system and multi-product production suites to ensure regulatory compliance, product quality, and efficient tech transfer. From early clinical supply to full commercial manufacturing, Minaris provides the infrastructure and expertise to accelerate advanced therapy programs.

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Minaris Services

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Minaris Advanced Therapies is dedicated to helping innovators in cell and gene therapy succeed. Whether you are in early-stage development or preparing for commercial launch, our end-to-end expertise, global reach and commitment to quality make us the ideal partner for cell and gene therapy manufacturing and GMP biosafety and analytical testing of all biologics.