Efficient, reproducible production of mRNA-based medicines depends on a well-designed continuum spanning plasmid DNA (pDNA) preparation, in vitro transcription (IVT), and lipid nanoparticle (LNP) formulation. In this session, expert speakers will outline how targeted process choices at each stage can significantly improve yield, reduce impurity burden, and simplify downstream development.
Attendees will discover how lysis strategies influence pDNA recovery, what parameters most directly affect IVT reaction performance, and how capture and polishing steps can maximize mRNA purity. The speakers will highlight chromatographic approaches that enable both purification and characterization of increasingly complex LNP formulations. Collectively, these insights will provide a roadmap for developing nucleic acid processes that are scalable, robust, and aligned with regulatory expectations.
Attend this webinar to:
You have registered for this webinar