Newsletter | July 16, 2025

07.16.25 -- Fix Your CGT Launch Plan: Speed Isn't the Problem. Strategy Is.

The Next Frontier: Industrializing Cell Therapy Manufacturing

Learn how leveraging platform processes can enable flexible service at each level – pre-clinical through commercial – and reduce development timelines and costs on the path to market.

 

Feasibility That Prepares You For Clinical Success

Delve into why investing in a comprehensive feasibility program for GOI testing is not just beneficial, but absolutely essential for cell and gene therapy companies.

 

Fast Lane To Market: A 3-Stage Exploration Of Process Development

Designing a CGT production process that is scalable and repeatable at cGMP quality is complex, but your journey can be eased by following the right strategy and working with an experienced partner.

 

Cell Therapies: 3 Strategies For Creating A Cost-Effective Program

There is a significant opportunity for NK cell-based therapies to continue to make a significant impact in patient care. Discover strategies for creating a cost-effective NK cell biopharma product.

 

Cell Line Development For AAV

As advanced therapies race forward, staying ahead is paramount. Harnessing technology, sponsors can unlock efficiencies and propel production to new heights.

 

New Scale Down Models To Get Vectors To GMP Stages

These models are essential to process development as they allow developers to fine-tune each step without large investments in materials and consumables. Explore how to shorten timelines and advance your therapy to the clinical stage with speed and reduced costs.

 

IN THE NEWS

Manufacturing The First FDA Approved Gene Therapy For Early-Onset MLD

AGC Biologics Expands Cell Therapy Development Operations To Asia To Serve Growing Market Need

SOLUTIONS

Viral Vector Capabilities

Our scientists have extensive experience in viral vector-based gene therapy, specializing in adeno-associated viral vectors (AAV), lentiviral vectors (LVV), and retroviral vectors (RVV). We develop and manufacture viral vectors that meet commercial demands for gene therapy products.

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Services Supporting Every Stage Of The Product Journey

Our teams of scientists offer cell culture and cell modification in process development, with 30 years of cell therapy manufacturing and regulatory experience, including bringing three commercial products to market.

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