Licensing

ENABLING NEXT GENERATION CURES

The new possibilities with advanced, novel therapeutics have transformed the way pharmaceutical and biotech companies have approached drug discovery and development. With the surge in immunologic, cell and gene therapies, we are pleased to offer a comprehensive, validated, and broad range of licensing opportunities that can help you develop a robust, innovative pipeline.

We are here to support you whether you decide to in-license technologies, develop an in-house processing capability, scale manufacturing, or de-risk regulatory approvals.

Our long-term commitment, attention to details and result-oriented approach, with years of experience in developing and handling highly complex biological materials such as viral vectors, cell lines, and gene modulation and editing technology can help bring your therapy to market.

For research use only. Not for use in diagnostic procedures.

Explore Our Solutions

Gene Expression System

The CHOSOURCE™ GS KO expression platform is designed to streamline the biotherapeutic manufacturing process, reducing costs and timelines while improving consistency and reproducibility.

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Transduction Enhancer for Cell Therapy

Elevate cell therapy projects with the proprietary, robust, efficacious, GMP-grade, LentiBOOST® lentiviral transduction enhancer

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AAV Capsid Development

Providing clinically optimized and validated AAV expression capsids to address vector dosage, immunogenicity, and tissue tropism challenges.

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Pin-point™ Base Editing Platform

Providing broad access to base editing, the new generation of CRISPR-Cas9 genome editing with improved accuracy and safety, across the research and therapeutic markets with licenses and Pin-point™ Base Editing products and services.

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Ad19 Adenoviral Vector Manufacturing

Streamline your workflow efficiencies and reduce manufacturing bottlenecks with the Ad19 adenoviral manufacturing solution.

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Featured Resources

Ebook

Cell and Gene Therapy: Guiding the Way to Precision Treatment

Cell and Gene therapies are leading the way toward breakthrough treatments for today’s untreatable diseases. See how you can advance your cell and gene therapy projects from ideation to implementation.

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Infographic

Generate the best-in-class viral vectors

The surge in gene therapy clinical trials require optimized viral vector design, production and manufacturing. Download this infographic to learn ways we can elevate your gene therapy projects.

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Ebook

Your Pathway Toward CRISPR Workflows

CRISPR is transforming research by enabling the modulation of hundreds or thousands of genes in a single experiment. This solution guide will help you confidently navigate the path toward more efficient CRISPR workflows.

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