What’s Happening 
in AAV Gene Therapy Now

Live30 webinars are thirty-minute presentations designed to update you on the latest innovations, applications, and data in a fast yet interactive format.

Recombinant adeno-associated virus (rAAV) vectors have become essential in gene therapy for delivering therapeutic genes effectively. However, the challenge of separating empty capsids from...

Revolutionizing recombinant adeno-associated virus (rAAV) characterization, Viralgen’s poster presents how high-throughput sequencing (HTS) enables detailed insights into rAAV product integrity,...

Navigating the complexities of Chemistry, Manufacturing, and Controls (CMC) regulations is critical for advancing gene therapies. Viralgen’s latest poster highlights their innovative approach to...

High-throughput sequencing (HTS) is transforming recombinant adeno-associated virus (rAAV) characterization, and Viralgen's latest poster showcases cutting-edge methodologies for deeper insights into...

In the rapidly evolving field of gene therapy, optimizing the production of adeno-associated viral vectors (AAVs) is essential for success. Our latest white paper dives into the advantages of using...

Innovations in adeno-associated virus (AAV) manufacturing are shaping the future of gene therapy, and Viralgen's recent scientific poster highlights a groundbreaking approach. The study demonstrates...

In the rapidly evolving field of gene therapy, process optimization is key to success. Viralgen's latest poster reveals how multivariate data analysis (MVDA) enhances upstream AAV vector...

Viralgen relies on a proprietary manufacturing platform, advanced applications of data, and broad experience to accelerate production

Discover how Viralgen's Regulatory Affairs team drives faster speed to clinic and improved product quality through proactive collaboration with customers and regulators. This whitepaper explores how...

Explore how TAAV and Viralgen simplify rAAV manufacturing with neDNA™ and the Pro10™ platform. This whitepaper highlights how these innovative technologies accelerate gene therapy development, reduce...

Discover key strategies for overcoming variability and scalability challenges in AAV production for gene therapy. This poster by Viralgen highlights comparability studies, process changes, and...

As gene therapy continues to evolve, overcoming the variability and scaling challenges in AAV manufacturing is crucial for the production of safe and effective treatments. Manufacturers face...

This study highlights the importance of monitoring viral capsid protein charge distribution in AAV gene therapy vectors to ensure product quality. Using imaged capillary isoelectric focusing (icIEF),...

Navigating regulatory challenges with Viralgen’s head of regulatory affairs María Orío

The rapid advancement of cell and gene therapies offers unprecedented potential to treat complex diseases, but navigating both scientific and financial challenges remains a significant hurdle. From...

This study compares the production of recombinant AAV vectors using traditional plasmid DNA and neDNA™, a linear DNA molecule free of bacterial sequences. Evaluating both methods in Viralgen’s Pro10™...

Viralgen leverages its Pro10™ production platform to manufacture high-quality AAV6 vectors, enabling efficient, large-scale production for cell therapies. With broad tropism, high transduction...

Viralgen offers specialized production of Adeno-Associated Virus (AAV) gene therapy vectors, using a proprietary suspension and triple transfection platform. Our scalable 2000L manufacturing process...

Successful technology transfer is essential for scaling gene therapy manufacturing processes from clinical to commercial stages. This poster highlights Viralgen’s proven methodology for ensuring a...

Despite recent advances in the gene therapy field, significant challenges lie ahead for the consistent manufacturing and release of these medicines. rAAV particles are built from the folding of three...

Viralgen developed a dedicated platform and a designed-for-use cell line, which combine to improve efficiency and reduce costs

Join this webinar to examine scale-up optimizations of AAV gene therapy in upstream processing. The featured speaker will explore both process characterization and experimental approaches to better...

Discover how the HEK293-derived Pro10™ cell line accelerates AAV vector production. This whitepaper explores a scalable, animal component-free platform that reduces process development time and...