The cell therapy industry is transitioning toward standardized production by implementing closed, automated, and modular platforms to overcome the inherent variability of disparate manufacturing processes. For developers and tech professionals, this shift necessitates the integration of process analytical technologies, electronic batch records, and AI-driven predictive controls to ensure reproducibility and optimize culture conditions in real time. These digital transformations will ultimately lower costs and reduce reliance on end-point testing through data-driven quality predictions.
Read the full article at Genetic Engineering News
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