Newsletter | August 11, 2026

08.11.26 -- Solving Vector Yield Challenges Starts Long Before Manufacturing

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Webinar: Evolving Lentiviral Vector Manufacturing with Stable Production

As in vivo lentiviral programs expand, manufacturers need scalable, reliable production platforms that deliver consistent quality. Join Asimov's Sybil Danby and Adam Carcella to explore next-generation LV manufacturing strategies, including producer and packaging cell lines, and learn how synthetic biology and computational modeling are improving titer, reducing variability, and accelerating development for both ex vivo and in vivo therapies. Click here to learn more.

FOCUS ON MANUFACTURING

Solving Vector Yield Challenges Starts Long Before Manufacturing

Cell & Gene Live panelists take a deep dive into why solving vector yield challenges begins with early biological and manufacturing decisions rather than process optimization alone.

Comprehensive Characterization Of Oligonucleotides And Related Impurities

A two-dimensional LC/MS strategy improves the separation of coeluting oligonucleotide impurities. High-resolution sampling and automation enable deeper characterization of low-level variants.

Reliable, Quality Design Proven Through Stress Testing

Rigorous multi-cycle stress testing and environmental validation ensure manufacturing hardware delivers uncompromising reliability for critical processing workflows.

How Enzymatic Synthesis Is Transforming Nucleotide Production

From harsh chemicals to gentle enzymes, explore the groundbreaking shift in nucleotide synthesis, making drug manufacturing cleaner, greener, and more efficient.

Enhancing Cryopreservation Strategies For Small-Volume ATMPs

Discover best practices for cryopreserving small-volume ATMPs, focusing on sterility, viability, and efficiency with advanced containers and packaging.

Clearing The Path To Approval: Residual Reagent Control In AAV Gene Therapy

Stricter regulatory expectations for AAV therapies demand robust control of residual transfection reagents, comprehensive documentation, and proactive quality strategies to avoid costly development delays.

Extrahepatic Delivery Of mRNA-LNP To Spleen

In vivo CAR-T approaches aim to reprogram T cells directly in the body using targeted lipid nanoparticles. Improved delivery to immune organs highlights new potential for scalable cell therapies.

Extracellular Vesicle Isolation From Conditioned Media

Examine a scalable, sterile solution for isolating extracellular vesicles (EVs) in exosome therapeutics to enhance yield, purity, and commercial viability through innovative filtration technology.

Streamline Biopharmaceutical Manufacturing With Versatile Platforms

Gain insights into how standardized quality controls, robust analytics, and streamlined processes can improve efficiency, reliability, and scalability across the development lifecycle.

Applying Next Generation Sequencing To Accelerate CGT Product Development

Next Generation Sequencing (NGS) revolutionizes gene therapy by enhancing the development and safety of viral vectors like AAV and lentivirus. Discover more about its impact.

Optimizing AAV8 Capsid Purification With Oversized GOI

Strengthen AAV gene therapy quality and regulatory compliance. Modern AEX purification strategies achieve over 90% full capsid purity, even for oversized AAV8 vectors.

Building A Scalable Global T Cell Manufacturing Platform

Achieve scalable T cell manufacturing with automation, standardized workflows, and integrated quality control to enable high-yield production, flexible scheduling, and seamless tech transfer.

MANUFACTURING SOLUTIONS

Optimize Protein Purification Using Filtration Solutions - Cytiva

Advanced Magnetic Cell Separation System - Thermo Fisher Scientific Bioproduction

Adherent Cell Platforms For Scalable Viral Vaccine Manufacturing - Corning Life Sciences

Contract Develop, Manufacture, And Technology Solutions - FUJIFILM Biotechnologies

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