Newsletter | July 24, 2025

07.24.25 -- Essential Steps For A Successful Analytical Tech Transfer

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Join the 10th Anniversary of the CAR-TCR Summit to reflect on a decade of progress whilst engaging in solutions-driven discussions that will empower you to tackle cell therapy development challenges to help shape the future of the field. You’re guaranteed to leave with actionable solutions to combat the challenges currently halting your therapeutic development and effectively translate your cell therapy from bench to bedside.

FOCUS ON OUTSOURCING

Essential Steps For A Successful Analytical Tech Transfer

Biologics tech transfer means sharing up to 20 assays. Miss a step, and you risk delays, bad data, and products stuck in limbo.

From Innovator To Partners In Cell Therapy: Our Evolution Into A CDMO

Explore the common pitfalls encountered in CGT CDMO collaborations, including communication breakdowns, differing regulatory interpretations, and program prioritization challenges.

Part Two: Overcoming Limits In LVV Titer Measurement

Learn how a platform streamlines LVV titer measurement, offering a faster and more efficient alternative to traditional methods and addressing key process development challenges.

Optimization Of rAAV Production Using An In-House Suspension HEK293 Cell Line

Boost rAAV yields and quality while reducing costs with our proprietary HEK293 cell line and scalable, optimized manufacturing platform for gene therapy.

Evaluating BACS For T Cell Isolation In CAR-T Manufacturing

Consider how Buoyancy Activated Cell Sorting (BACS) can streamline T cell isolation, reduce costs, and enhance CAR T and TCR cell therapy manufacturing — access the full study to learn more.

Unlocking Flexible AAV Production With In-House Plasmids

Discover how 3PBIOVIAN’s advanced plasmid manufacturing and AAVion® platform can drive your AAV program forward by reducing production costs while maximizing efficiency.

Caring Cross: Boro Dropulić's Big Idea That Might Change The World

With real-world examples and a vision that challenges the prevailing norms of biotech commercialization, this conversation offers a powerful look at what it takes to reshape the future of healthcare.

Optimizing Biotherapeutic Protein Expression With CHO Vector Technology

Explore a high-strength synthetic gene promoter that boosts titers while preserving product quality and expression stability for more efficient biomanufacturing.

Development Strategies For Adenovirus-Based Gene Therapies

Scaling up viral vector production can be challenging, and ensuring consistent titers and activity requires careful optimization and technical expertise.

Comprehensive GMP Manufacturing Of mRNA-LNP Drug Products

Learn how delivering a comprehensive CMC package under a single manufacturer can help to minimize the logistical complexity of multiple vendors that leads to major risks for RNA program success.

OUTSOURCING SOLUTIONS

Kincell Bio Capacity Update April 2025: Cell & Gene Therapy - Kincell Bio

ATP Detection By Quantitative Mass Spec Imaging (QMSI) - Aliri Bioanalysis

Novartis Contract Manufacturing Services Capacity Update October 2024: Fill/Finish - Novartis Contract Manufacturing

Enabling The Outcome In EMEA - Cryoport Systems

Accelerating CGT With Speed, Cost, And Innovation Advantages - VintaBio

EVENTS

Advancing the Future of Cell & Gene Therapy

This 11-12 November, Cell 2025 unites 1,000+ leading experts across the CGT value chain to solve key challenges, from scalable bioprocessing and regulatory hurdles to accelerating development timelines.

 

Gain practical strategies across cell culture, therapy development, and CGT manufacturing, and hear from world-renowned leaders Bobby Gaspar (CEO, Orchard Therapeutics), Christof Von Kalle, (Director & BIH Chair, Research Clinic Luxemburg), and Dame Molly Stevens (University of Oxford). Register Now

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