Newsletter | October 5, 2026

10.05.26 -- Enzyme Activity As A Surrogate Potency Marker In Cell Therapy

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Webinar: Viral Vector for Rare and Ultra-rare Disease

Rare and ultra-rare disease programs require viral vector strategies tailored to smaller patient populations. Explore practical approaches to right-size development and manufacturing, determine appropriate scale, reduce costs and timelines, and align processes with clinical and commercial needs. This webinar will share practical strategies for leveraging manufacturing partners and advancing toward proof of concept and clinical validation efficiently and cost-effectively. Click here to learn more.

FOCUS ON OUTSOURCING

Enzyme Activity As A Surrogate Potency Marker In Cell Therapy

When measuring cell therapy potency, biochemical assays can provide a rapid alternative to the time- and material-consuming standard of cell-based assays.

 

 

Optimized Transient Transfection Platform: AAV Program From Gene To GMP

Achieve faster AAV gene therapy progress by adopting a unified platform for manufacturing. Accelerate your program to GMP readiness with up to 9x higher titers and robust, high-quality full capsid yields.

 

What's The Greatest Risk For CDMOs Ahead?

Economic volatility, regulatory uncertainty, and capacity constraints pose major risks to CDMOs, threatening growth, profitability, and long-term sustainability in an increasingly competitive global market.

 

Standardized Workflows: The Key To Scaling Modern Gene Therapies

Platform-based manufacturing uses standardized, pre-qualified workflows and analytics that reduce variability, simplify regulatory submissions, and accelerate the path to commercial success.

 

Managing CMC Risk For Complex Peptide And Nucleic Acid Therapeutics

At TIDES USA 2026, experts discuss how formulation science, stability strategies, and advanced analytics help reduce CMC risk and enable confident development of peptide and nucleic acid therapeutics.

 

Flaws In Platform Processes For Cell And Gene Therapy Progress

Standard platform processes promise speed and consistency in CGT development, but biological variability and evolving program needs often expose their limitations.

OUTSOURCING SOLUTIONS

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Strategically Developing Cell Therapy Innovations From Lab To Market - Kincell Bio

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Built On Stability, Committed To Your Success - SK pharmteco

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Advanced iPSC Workflows: Accelerating Cell Therapy Development - Catalent

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