We're proud to receive a 2025 CDMO Leadership Award in the “Small Molecule Dosage Form - Global" category.
From global life-saving vaccines to personalized cancer therapies, messenger ribonucleic acid (mRNA) is being considered for a variety of clinical applications, creating diverse requirements for scale and dosage. To meet these varying needs, flexibility in the manufacturing process is critical, as drug developers must determine how to efficiently deliver high yields of quality mRNA while also balancing logistical and financial objectives.
Partnering with an adaptable and collaborative CDMO can be essential to navigating industry challenges and finding the best solution to bring your unique mRNA vaccine or therapeutic to market. In a recent webinar, we explored options within a standard mRNA/LNP manufacturing workflow and highlighted Thermo Fisher Scientific innovations to support varying production strategies and enhance your processes, including: