Southern RNA
BRISBANE

Southern RNA Facilities

Our operations span two specialised facilities in Queensland, supporting the full lifecycle of RNA development. Our GMP Manufacturing Labs in Eight Mile Plains, Brisbane are purpose-built for GMP-compliant production and early clinical manufacturing, integrating advanced GMP-aligned suites with in-house analytical capabilities to ensure quality, compliance, and scalability. Complementing this, our R&D Innovation Labs at Nexus Way, Southport (Gold Coast) focus on research, process development, and translational science, providing a collaborative environment for biotech innovators and clinical partners.
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Cohort Innovation Space

16 Nexus Way, Southport QLD 4215
info@southernrna.com.au
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Brisbane Technology Park

37 Brandl Street, Eight Mile Plains QLD 4113
info@southernrna.com.au
FACILITY CAPABILITIES

Advanced Infrastructure for RNA Manufacturing

The Brisbane facility is designed to support end-to-end RNA programmes, from early R&D to GMP-aligned and clinical-grade production. Key capabilities include:

Dedicated R&D laboratories for construct optimisation and assay development

GMP-compliant production suites with scalable manufacturing

Integrated analytical laboratories for quality control and validation

Controlled documentation and traceability systems

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.

Frame (3)
01.

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.

Frame (2)
02.

Test & Release

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

FAQS

Your Questions Answered

Our FAQ section addresses the most common technical and compliance queries, providing clarity on our capabilities, processes, and quality systems.

Yes, our facilities produce GMP-aligned and clinical-grade mRNA and plasmid DNA suitable for early-phase trials.

We follow GMP-aligned processes, robust documentation, and quality oversight to meet regulatory expectations and support submissions.

We offer flexible production from milligram-scale research material to multi-gram clinical-grade batches.

Yes, our in-house analytical team supports identity, purity, impurity profiling, and stability testing across all projects.

Absolutely. Our team develops reproducible processes for smooth transition from research-scale to GMP-aligned clinical production.