Platform Technology
Flexible mRNA and plasmid DNA platforms built to scale with your program, from early research through clinical readiness.
Flexible mRNA and plasmid DNA platforms built to scale with your program, from early research through clinical readiness.
One partner from sequence design to release-tested material: process development, manufacturing, and analytics under one roof.
A multidisciplinary team spanning nucleic acid chemistry, molecular biology, and process development stands behind every project.
As an Australian manufacturer, your eligible R&D spend with Southern RNA may qualify under the Australian Government’s R&D Tax Incentive.
Researchers and biotechnology companies use Southern RNA’s plasmid DNA and mRNA production platforms to generate high-quality raw materials for gene expression studies, vaccine design, and therapeutic candidate evaluation. This includes capped, modified mRNA and traceable pDNA templates for in vitro and in vivo applications.
Preclinical programs benefit from scalable production of research and GMP-aligned grade nucleic acids as they advance toward translational milestones. Southern RNA’s process development and analytical services help ensure consistency, purity, and suitability for later stages of evaluation.
Biopharmaceutical developers preparing for early clinical studies (FIH through Phase I/II) rely on Southern RNA’s GMP-capable workflows to produce clinical-appropriate drug substance. This includes plasmid DNA for viral vector manufacturing and mRNA for vaccines or cell therapies, with quality documentation supporting regulatory needs.
Scientists and quality teams use Southern RNA’s comprehensive analytical platform to characterise nucleic acid products, support method development, and validate stability and release assays. This underpins confidence in product performance and regulatory compliance throughout development.
Southern RNA provides plasmid DNA and mRNA services, merging flexible manufacturing with advanced analytics. Our team supports scalable, high-quality nucleic acid production for therapeutic programs.
We provide plasmid DNA (pDNA) and mRNA production using flexible platforms that deliver high-quality R&D and GMP- aligned grade materials at scalable volumes.
We provide a comprehensive nucleic acid analytical platform, supported by the deep expertise and experience of our multidisciplinary scientific team.

Southern RNA provides high-quality plasmid DNA and mRNA products for research and clinical applications. Our scalable production ensures consistent quality and performance, helping scientists accelerate RNA-based therapies.
Discover our co-transcriptional capping reagent for mRNA and lower the cost of your IVT.
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.
Australia offers a world-class environment for early-phase clinical studies, with GMP-capable facilities, experienced scientific teams, and comprehensive analytical capabilities ensuring high-quality plasmid DNA and mRNA at scale.
With clear regulatory frameworks, robust documentation standards, and streamlined submission processes, Australia provides a reliable pathway from research to first-in-human trials, helping de-risk timelines and accelerate progression from lab to clinic on the global stage.
Southern RNA’s platforms combine scalable manufacturing and analytics for high-quality plasmid DNA and mRNA production. Our technologies accelerate development while ensuring control and quality for clinical progression.
Production of high-quality plasmid DNA for use as IVT template and as starting material for advanced therapy programs. Linearisation, purification, and quality control are scaled to your development stage.
Co-transcriptional capping using Southern RNA’s Co Cap™ A reagents delivers high capping efficiency in a single IVT step, lowering cost and complexity versus enzymatic post-capping.
A comprehensive nucleic acid analytical suite covering identity, purity, integrity, and content, supporting method development, in-process control, and release and stability testing.
Systematic optimisation of IVT and purification processes for reproducibility and yield, with efficient scale-up from milligram research quantities to gram-scale batches.
Hear from partners and collaborators who’ve advanced their programs with Southern RNA.
“Partnering with Southern RNA dramatically accelerated our timeline from concept to GMP-ready material. Their team’s expertise and responsiveness were invaluable.”
Clinical Development Lead
Biotech Partner
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