Southern RNA
SCALABLE, GMP-READY RNA SOLUTIONS

Australia’s Advanced mRNA Manufacturing Partner — From Discovery to GMP Clinical Supply

Southern RNA provides end-to-end mRNA development, GMP manufacturing, and CDMO services, helping biotech innovators accelerate personalised medicines from early research through to clinical-grade production.

EXPLORE SERVICES
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Platform Technology

Flexible mRNA and plasmid DNA platforms built to scale with your program, from early research through clinical readiness.

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End-to-End Support

One partner from sequence design to release-tested material: process development, manufacturing, and analytics under one roof.

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Top Talent

A multidisciplinary team spanning nucleic acid chemistry, molecular biology, and process development stands behind every project.

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Tax Incentive

As an Australian manufacturer, your eligible R&D spend with Southern RNA may qualify under the Australian Government’s R&D Tax Incentive.

USE CASES

Solutions for Biotech Innovators & Therapeutic Developers

Southern RNA meets diverse scientific and biopharmaceutical needs with high-quality nucleic acid products and services that accelerate RNA technology development.

ENQUIRE NOW
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Biotech and Pharma R&D

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.

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Preclinical Development

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.

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Clinical Supply Enablement

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.

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Analytical and Quality Testing

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.

SERVICES

RNA Development & Manufacturing Services

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.

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Develop & Manufacture

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.

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Test & Release

We provide a comprehensive nucleic acid analytical platform, supported by the deep expertise and experience of our multidisciplinary scientific team.

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PRODUCTS

High-Quality RNA & DNA Solutions

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.

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mRNA

Southern RNA provides starting material for ATMP GMP manufacturing.

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Co Cap™ A

Discover our co-transcriptional capping reagent for mRNA and lower the cost of your IVT.

WHY US

Australia-Based, Globally Oriented

Southern RNA combines local scientific strength with international standards in mRNA and nucleic acid production.

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Phase-appropriate, scale-flexible CDMO platform

Integrated mRNA manufacturing and analytical testing processes designed to scale efficiently from early development to clinical readiness.

WHY US
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Phase-Appropriate Quality Systems

Robust, stage-aligned quality documentation and controls that support development, tech transfer, and regulatory progression.

Phase-Appropriate Quality Systems
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Time-Critical Delivery

Streamlined workflows and responsive project management to meet tight timelines without compromising quality or compliance.

Time-Critical Delivery
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Deep Technical Expertise

Hands-on scientific support across nucleic acid design, synthesis, purification, and advanced analytical testing.

Deep Technical Expertise
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Regulatory-Focused Support

Comprehensive documentation and guidance aligned with clinical and regulatory expectations at every phase.

Regulatory-Focused Support
CLINICAL TRIAL
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Designed for Regulatory Progression

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.

PLATFORM OVERVIEW

Advanced Platforms Powering RNA Development

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.

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A flexible, scalable platform for the production of research and GMP-aligned grade mRNA, supporting a range of sequence designs, modifications, and capping strategies. Processes are optimised for reproducibility, purity, and efficient scale-up from milligrams to grams.

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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.

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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.

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A comprehensive nucleic acid analytical suite covering identity, purity, integrity, and content, supporting method development, in-process control, and release and stability testing.

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Systematic optimisation of IVT and purification processes for reproducibility and yield, with efficient scale-up from milligram research quantities to gram-scale batches.

TESTIMONIALS

Voices of Confidence

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