Newsletter | October 2, 2025

10.02.25 -- How You And Your CDMO Should Leverage Contamination Control Strategies

SPONSOR

 

 

Explore available capacity and capabilities from leading CDMOs specializing in cell and gene therapy at the Cell & Gene Therapy session of the Outsourced Pharma Capacity Update (Oct. 9). This virtual event covers services from cell sourcing to vector design, formulation, and GMP-compliant manufacturing. Through short, interactive presentations, gain insights and connect with CDMOs ready to support your needs. Open to biopharma companies, consultants, and investors seeking partners for advanced therapy programs. Save your spot today!

FOCUS ON OUTSOURCING

How You And Your CDMO Should Leverage Contamination Control Strategies For Competitive Advantage

It is no longer sufficient to just meet compliance requirements; a proactive, risk-based approach to contamination control is now a differentiating factor that enhances operational efficiency and more. For biotech companies evaluating CDMOs, this shift is critical.

 

 

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.

 

Generation Of A Universal AAV Packaging Cell Line For Commercial Manufacturing

Uncover the benefits of this CGMP-ready, stable AAV packaging cell line with proven expertise to reduce costs, streamline manufacturing, and make life-changing gene therapies more accessible to patients in need.

 

Innovation That Is Evolving The CGT Landscape In 2025

Explore how cell and gene therapy leaders are adapting to funding pressures, regulatory shifts, and global complexity by prioritizing scalability and strategic partnerships for long-term success.

 

Mastering The Journey From Initial Method Transfer To Successful Lot Release

A panel of experts share potential pitfalls and lessons learned from their many years of experience across a wide array of projects in the cell and gene therapy space.

 

Biotechnology: The Key To America's Next Manufacturing Revolution

Discover how a recent expansion into Western Pennsylvania is aiming to enable more biopharmaceutical firms to translate cutting-edge science and research into practical applications.

 

A Cost-Effective, High-Quality Alternative To Full cGMP Production Of Plasmid DNA

Find a more robust, less rigid alternative that mirrors nearly all of the oversight and quality standards of full cGMP production while relaxing certain commercial standards, helping to overcome early development hurdles.

SPONSOR

 

Webinar: Break the Cell Therapy Manufacturing Bottleneck with Day 0 Transduction, Day 3 Harvest

Cell therapies face manufacturing challenges due to slow, variable processes. This webinar with Dr. Carl June introduces Synecta™ T1 CDNPs, which accelerate T-cell activation, enable early transduction, and ensure high viability without extra cytokines. These nanoparticles mimic natural immune signals, simplify workflows, and work across donor and patient samples—offering scalable, flexible solutions to improve T-cell therapy production and clinical reach.

OUTSOURCING SOLUTIONS

Allogeneic And Autologous Cell Therapy CDMO Services - FUJIFILM Biotechnologies

Plasmid DNA Platform - 3PBIOVIAN

Fast-Track Your Advanced Therapy With A Scalable cGMP-Ready Process - Catalent

Seamlessly Delivering Your Virotherapy - Recipharm Advanced Bio

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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