Scalable CDMO Platform
Integrated mRNA manufacturing and analytical testing processes designed to scale efficiently from early development to clinical readiness.
We are an Australian CDMO specializing in nucleic acid products for therapeutic development. We provide scalable manufacturing to accelerate innovation from benchtop to bedside. Southern RNA has end-to-end capabilities for mRNA and DNA, using advanced bioprocessing technologies and a skilled workforce. Our goal is to be a leading, customer-focused supplier known for quality and efficiency.
At Southern RNA, science is our foundation. We are guided by precision, reproducibility, and continuous improvement, recognising that successful RNA development requires rigorous design, deep process understanding, and disciplined quality oversight.
We apply data-driven decision-making and structured optimisation to ensure every programme is supported by robust scientific evidence. By combining innovation with controlled processes, we help partners reduce risk, strengthen regulatory readiness, and deliver scalable, reliable RNA solutions.
Our mission is to advance RNA science by providing reliable development and manufacturing solutions that enable innovation to move from concept to clinic. We support researchers and companies through rigorous processes and a foundation of quality. By combining technical excellence with partnership, we aim to reduce risk and accelerate timelines for RNA therapeutics and vaccines.
We aim to be a leading RNA-focused CDMO known for scientific depth and reliability. Our goal is to enhance Australia’s biomanufacturing while supporting global innovators, fostering an ecosystem for advanced RNA technologies. Through ongoing improvement and quality commitment, we strive to shape RNA therapeutics and be a trusted partner in transformative medicines.
Integrated mRNA manufacturing and analytical testing processes designed to scale efficiently from early development to clinical readiness.
Robust, stage-aligned quality documentation and controls that support development, tech transfer, and regulatory progression.
Streamlined workflows and responsive project management to meet tight timelines without compromising quality or compliance.
Hands-on scientific support across nucleic acid design, synthesis, purification, and advanced analytical testing.
Comprehensive documentation and guidance aligned with clinical and regulatory expectations at every phase.
Meet our team of talented individuals, with an extensive track record in industry and manufacturing of nucleic acids products.