About Virax Biolabs
Advancing Immune Diagnostics for Chronic Inflammation and Immune Dysfunction.
Virax Biolabs is a Nasdaq-listed biotechnology company advancing immune-profiling technologies across research and diagnostics. Our lead diagnostics platform, ViraxImmune™, is initially being developed for post-acute infection syndromes, including Long COVID, with broader potential in immune monitoring and haemato-oncology as the platform evolves. Through ImmuneSelect, we also provide research-use products and services supporting T cell and immune-response profiling.
Meet Our Leadership
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Clinical relevance
Focused on meaningful diagnostic gaps and reducing clinical uncertainty.
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Scientific rigour
Grounded in T cell biology, structured evidence generation and certified quality systems.
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Disciplined execution
Advancing development through defined clinical, regulatory and commercial milestones.
Leadership & scientific advisory board
Experienced Corporate
& Scientific Leadership.
Virax Biolabs is guided by an experienced management team, Board of Directors and Scientific Advisory Board, with expertise spanning biotechnology, diagnostics, clinical development, regulatory strategy and commercialisation.
COMBINED EXPERTISE
Corporate execution informed by scientific depth.
Leadership and advisory perspectives are structured to connect laboratory development, clinical evidence, regulatory planning, and commercial decision-making.
Molecular diagnostics
Regulatory strategy
Biotechnology commercialisation
Clinical trial design
Quality & regulatory strategy
World-Class Operational Standards.
Virax Biolabs operates quality management systems certified to ISO 9001:2015 and ISO 13485:2016. ViraxImmune™ is being advanced through a staged development strategy comprising active UK clinical validation, a planned US laboratory-developed test pathway subject to laboratory readiness and applicable requirements, and a potential longer-term FDA IVD pathway.
Development and launch timing remain subject to clinical evidence, regulatory engagement, quality-system readiness, and operational progress.
Quality system
ISO 9001 & ISO 13485 Certified
Current quality system maintained under ISO 9001 & ISO 13485 certification for medical devices.
2027 target
Planned US LDT Pathway
Preparation aligned with applicable laboratory, CMS, and CLIA requirements, subject to development progress.
2028+ target
FDA De Novo / IVD Pathway
A potential route toward broader regulatory authorisation following clinical and analytical validation.
PARTNER WITH US
Start a Conversation.
Contact our team regarding clinical studies, scientific collaboration, commercial partnerships, media or investor relations. Your inquiry will be directed to the appropriate team member at our BioCity headquarters.
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Clinical Study-site and research inquiries02
Commercial Distribution and strategic alliances03
Corporate Media and investor-relations inquiries