Following a customer-centric approach, the main objective of VIVEbiotech’s Custom Solution & Process Development Department is to develop the most productive, functional and regulatory-compliant vector before the production phase in bioreactors, whether for ex-vivo and in-vivo administration.
Improve producer cell lines, including the possibility of genetic modification to:
Enhance productivity.
Increase tropism.
Optimize expansion.
Obtain a stable cell line.
Develop new analytical methods to:
Better understand our process and/or product.
Improve analytical methods for batch release.
Custom development of potency assays.
Different pseudotyping strategies.
Optimizing conditions to maximize yields.
Purification process optimization for peak performance.
Other areas of innovation:
Development of integrative and non-integrative vector systems.
Engineering and delivery of large trangenes.
Design and optimization across multiple lentiviral vector generations.
+ 10 in-vivo lentiviral vector programs, several in clinical development.
GMP-certified for clinical-grade release.
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