As momentum in the mRNA field shifts from pandemic response toward chronic disease applications, developers face converging pressures: funding constraints, evolving regulatory expectations, and growing investor and public skepticism. This panel brings together perspectives from established mRNA companies, emerging biotechs, and CDMO leaders to provide a frank, data-informed assessment of where the field stands – and, critically, what organizations can do about it.
Attendees will gain practical frameworks for navigating the current landscape, from de-risking clinical timelines to making informed decisions about when to partner with a CDMO versus building in-house capacity.
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Register now to gain the tools and perspectives needed to build a more resilient mRNA program ahead of 2026.