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SKyvec™ Viral Vector Platform

Our harmonized SKyvec™ viral vector platform is designed to streamline process development, manufacturing, and scale-up across AAV, lentiviral, and adenoviral vectors, supporting gene therapy programs from early development through clinical and commercial production. Backed by global development and manufacturing capabilities, this flexible platform approach can also be adapted to additional viral vector modalities, including oncolytic viruses, herpes-viruses, retroviruses, and emerging gene therapy applications.

Our integrated capabilities span cell line and plasmid development, process development, drug substance manufacturing, and drug product manufacturing. With operations across North America and Europe and experience supporting clinical-stage programs, SKyvec™ enables efficient progression from vector design to scalable manufacturing while maintaining process consistency, process quality, and supply continuity.

SKyvec™ Viral Vector Platform Solutions

SKyvec™ AAV

Our AAV platform supports multiple serotypes and transgenes with suspension and adherent approaches, enabling efficient and scalable development and manufacturing from early-stage through commercial supply with consistent and high-yield performance.

SKyvec™ Lenti

Our Lentiviral platform enables flexible manufacturing across adherent and suspension systems, supporting consistent performance and scalable production for a range of gene therapy applications, from ex vivo to in vivo applications.

SKyvec™ Adeno

Our Adenovirus platform supports gene therapy, vaccine, and oncolytic applications through adherent and scalable suspension processes, deep vector expertise, and a streamlined downstream architecture designed to maximize recovery, reduce complexity, and support commercial-scale production.

Analytical Services

Our Analytical Accelerator™ Testing Platform speeds time to CGMP batch release more than three-fold and conserves sample volumes needed for testing by up to 50 percent.

Release, in-process, and characterization services include:

Revolutionizing Lentiviral Vector Manufacturing for <em>In Vivo</em> and <em>Ex Vivo</em> CAR-T Cell Therapies_White-Paper

Featured Resource

Revolutionizing Lentiviral Vector Manufacturing for In Vivo and Ex Vivo CAR-T Cell Therapies

In vivo CAR-T therapies represent a new paradigm in immuno-oncology, where lentiviral vectors (LVVs) are delivered directly to the patient. Read our white paper to learn.

Related Resources

Viral Vector Events

BIO International Convention

San Diego, CA
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Cell & Gene Therapy Summit 2026

Boston, MA
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CPHI Milan

Milan
Italy
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ChemOutsourcing 2026

Boston, MA
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