Brochure | July 11, 2024

Take The Next Step In Your mRNA Product Journey

GettyImages-157291618 Scientist inspecting vial

The development of mRNA therapeutics and vaccines presents significant challenges for biotech companies transitioning to clinical and commercial manufacturing. These challenges encompass technical complexities, adherence to Current Good Manufacturing Practice (cGMP) regulations, and intricate logistical considerations. The fragmentation of manufacturing processes across multiple, independent partners further exacerbates these difficulties.

To effectively navigate this complex landscape and ensure successful cGMP manufacturing, a strategic partnership with an integrated Contract Manufacturing Organization (CMO) is paramount. Such a CMO should possess the expertise, facilities, and robust supply chains necessary to offer a complete manufacturing solution, encompassing all stages from plasmid DNA (pDNA) production to final fill-and-finish.

Learn how a collaborative approach significantly mitigates risk associated with mRNA product manufacturing and fosters greater agility and speed throughout the development process, while guaranteeing consistent production of high-quality mRNA therapeutics and vaccines at an optimal cost.

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Novartis Contract Manufacturing