Newsletter | April 28, 2025

04.28.25 -- Navigating Tariffs: Implications And Strategies For Pharmaceuticals Manufacturers

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The ISCT 2025 Scientific Annual Meeting (May 7-10 in New Orleans) is the largest global gathering for KOLs and subject matter experts for driving the clinical translation of cell and gene therapies. The work presented at this conference spans regulatory affairs, workforce development and the entire development pathway from pre-clinical work to Phase 3 clinical trials, CGT product launch and market access. Register Today!

FOCUS ON OUTSOURCING

Implications And Strategies For Pharmaceuticals Manufacturers

The U.S. tariffs on trading partners bring a whole new set of challenges, but there are tactics and strategies companies can deploy to help offset the cost and operational impacts. 

Plasmid Impurity Sizing Of nptII In rAAV By ddPCR

Explore our ddPCR method for assessing plasmid-derived antibiotic resistance gene impurities in rAAV products to enhance regulatory compliance and ensure the safety and quality of gene therapy vectors.

Deamidation Drives AAV9 Potency Loss

This study aims to identify the cause of AAV9 potency loss observed during short-term storage at elevated temperatures and long-term refrigeration.

Revolutionizing Viral Vector Production With Intensified Cell Culture

Intensified adherent cell culture offers a promising solution to the limitations of traditional suspension culture, with the potential to improve efficiency, reduce costs, and accelerate development.

Advancing Immune Cell Therapies And Overcoming Cost Challenges

Immune cell therapies have incredible potential for cancer treatment, and making them more cost effective is a critical consideration for improving patient access and outcomes.

Engineered Plasmids And Optimized HEK293 Cells Boost AAV Yield

Low AAV yields and absent platform processes raise production costs—discover a scalable suspension-based solution.

Delivering AAV Therapies Via Candidate Screening And Feasibility Studies

Partnering with an experienced CDMO early can ease funding challenges and secure clinical material for AAV research.

An End-To-End Industrialization Roadmap For Autologous Cell Therapy

Explore specificities and challenges, leveraging automation for scalability with the Cocoon® Platform, and building a vein-to-vein network to achieve ‘just-in-time’ delivery of therapies.

Best Practices For Oncolytic Virus Design, Development, Manufacturing

Oncolytic viruses have the potential to revolutionize standard cancer treatment, but their continued progress hinges on meeting a number of goals linked to safety, efficacy, and commercial scale-up.

OUTSOURCING SOLUTIONS

Overcome CRISPR's Limitations With TARGATT Gene Knock-In Technology - Applied StemCell

Cell & Gene Therapy Preclinical Testing Solutions - Labcorp Cell and Gene Therapy Solutions

Viral Vaccine Lot Release Package - WuXi Advanced Therapies

RNA Therapies - ReciBioPharm

Services For Advancing mRNA-LNPs From Bench To Clinic - Cytiva

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