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"Maximizing therapeutic ROI: How to boost lentiviral vector production"

This infographic outlines four key questions to evaluate lentiviral vector platforms and CDMO partners for maximizing therapeutic ROI.

Cell and gene therapy developers face growing pressure to balance cost-efficiency with performance as lentiviral vector production becomes more complex and expensive. With longer development timelines and stricter regulations, choosing the wrong production platform or CDMO partner can lead to costly delays, tech transfers, and regulatory setbacks.

This infographic offers a strategic framework for evaluating lentiviral vector platforms and CDMO partnerships to maximize ROI. By addressing four critical questions, biopharma innovators can identify solutions that ensure superior performance and cost-efficiency from preclinical to commercialization. Access:

• Criteria for balancing cost-efficiency with high-performance titers and yields
• Factors for seamless scalability from development to commercial production
• Considerations for regulatory compliance and long-term program success

Offered Free by: BioPharma Dive's studioID and MilliporeSigma
See All Resources from: BioPharma Dive's studioID and MilliporeSigma