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Xtalks, Online
2025-11-20
The production of cell and gene therapies faces stringent regulatory requirements that demand the use of high-quality, animal-free raw materials to ensure patient safety and product consistency. Many manufacturers struggle to find reliable, compliant materials that also perform well in critical applications. This webinar will address these challenges by exploring validated solutions that help meet regulatory expectations while maintaining performance using animal-free materials.
Recombinant insulin supports cell proliferation and enables the development of chemically-defined media formulations essential for cell therapy manufacturing. Additionally, insulin plays a vital role in viral vector production for gene therapy, resulting in significant improvements in AAV titer and enhanced viral encapsidation in HEK 293 cells.
Additionally, recombinantly produced trypsin eliminates the contamination risks inherent in animal-derived trypsin and ensures consistent enzymatic activity while maintaining excellent cell viability and essential surface markers during passaging procedures, making it an ideal solution for cell therapy manufacturing workflows.
A recent study evaluated the performance of both recombinant insulin and trypsin in mesenchymal stem cell cultures, demonstrating that insulin effectively stimulates cell proliferation while trypsin nicely maintains cell viability and phenotype during dissociation, together meeting the rigorous standards required for therapeutic manufacturing applications.
The featured speaker will demonstrate how these validated animal-free solutions can transform manufacturing processes, offering practical insights into optimizing both cell and gene therapy production while ensuring regulatory compliance and cost-effectiveness.
Register for this webinar to explore how animal-free raw materials support regulatory compliance and optimize CGT manufacturing performance.
Keywords: AAV, Animal-Free, Cell & Gene Therapies, Cell Culture, Cell Therapy Manufacturing, Commercial Manufacturing, Drug Development, Insulin, Quality, Regulatory, Regulatory Compliance, Therapeutic Areas
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Organized by:
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Xtalks |
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Invited Speakers:
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Sara Bursomanno, PhD, Senior Global Product Manager, Novo Nordisk Pharmatech A/S
Chantale Julien, Global Product Manager, Novo Nordisk Pharmatech A/S
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Deadline for Abstracts:
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2025-11-20
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Registration:
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Free Registration
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E-mail:
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tristan@xtalks.com
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