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 costs, meeting growing clinical and commercial demands for gene therapies.
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February 06, 2023
White paper: A proprietary mammalian suspension technology for scalable rAAV production: The Pro10™ cell line
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Resources
Webinar: Exploring key regulatory considerations to ensure patient safety in the gene therapy space
In July, a panel of expert speakers—Christine Lebec (Sensorion), Leigh Shaw (SpliceBio), Nathalie Clement (Siren Biotechnology), and María Orío (Viralgen)—came together to explore the evolving regulatory landscape in the cell and gene therapy (CGT)...
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July 09, 2025

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Viralgen Joins Orphan Therapeutics Accelerator Clinical Development Network as a Manufacturing Partner to Advance Rare Disease Therapies
Viralgen brings strong AAV gene therapy manufacturing capabilities to growing group of partners supporting new model for developing and commercializing orphan drugs Boston, MA & San Sebastian, Spain - May 14, 2025 – Orphan Therapeutics Accelerator...
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May 14, 2025

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Viralgen collaborates with Trogenix to advance AAV gene therapy for glioblastoma
Viralgen accelerates clinical development process: scaling manufacturing and completing GMP production of Trogenix’s AAV gene therapy in under 12 months. San Sebastián, Spain, 6 May 2025 – Viralgen, a leading contract development and manufacturing...
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May 06, 2025