Navigating the Regulatory and Manufacturing Realities of mRNA Therapeutic Development

The regulatory and manufacturing challenges of the increasingly dynamic and multifaceted landscape of mRNA therapeutics prompts forward-looking discussions

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Cytiva eBook cover January 2025Introduced to the public in the form of the COVID vaccines, mRNA technology is based on decades of research. Still in the early phases, the next-generation of these therapeutics will expand beyond vaccine applications into additional disease states and showcase the technology’s prowess. But challenges remain. No common manufacturing platform currently exists and a regulatory framework is still being defined. In a recent GEN webinar, a panel of industry experts explored the evolution of mRNA technology and the innovations that are driving the conversation around manufacturing setups and regulatory decisions.