
Partner with World
Leaders in Molecular Multiplexing
From custom diagnostics to co-development — we collaborate to create molecular multiplexed solutions that deliver more
Why spend years developing multiplexing capabilities when you can partner with us and access proven technology already transforming diagnostics globally?
With 15+ years of molecular multiplexing innovation and 100+ patents, SpeeDx can tailor solutions to your needs. From initial assay design through regulatory approval and commercial manufacturing, we've successfully delivered solutions for partners globally across every stage of the development journey.
Leaders in PCR Multiplexing
SpeeDx technology has been used for molecular diagnostics across 100+ laboratories in 30+ countries. Our ResistancePlus® and PlexPCR® assays process hundreds of thousands of samples annually, while providing cost-effective solutions for laboratories.
Proven at Scale
The SpeeDx R&D and Innovations development teams are highly knowledgeable and skilled assay developers. These experts love the challenge of a new project and apply a rigorous, hands-on approach to find the best solution to meet your needs.
Experienced Developers
Where competitors have lengthy timelines for multiplex assay development, our proprietary PlexPrime® and PlexZyme® technologies enable streamlined development cycles from concept through to validated assays. Along with our scale-up manufacturing expertise, we have your needs covered.
Rapid Development Timelines
Our team has navigated compliance across global regulatory frameworks for multiple product lines. We deliver technical validation packages under our ISO-13485 compliant frameworks for seamless integration into your regulatory dossiers.
Regulatory Expertise You Can Trust
Whether you need custom diagnostics or research assays, tests developed for your preferred instrumentation, or co-development of novel assays, we structure partnerships around your strategic objectives and commercial timelines.
Flexible Partnership Models
Why Partner with SpeeDx?
Benefit from the powerful PCR technologies and product development expertise at SpeeDx and enjoy a consultative approach to assay design. Each partnership model is unique—tailored to your strategic goals, risk tolerance, and commercialization plans—creating mutual value and long-term competitive advantages.

Let us accelerate your journey
Whether you're a reference laboratory requiring custom solutions, a diagnostic company seeking competitive advantage through proven multiplexing technology, or a pharmaceutical company interested in novel assay development, our expert team delivers end-to-end support from concept through commercial readiness.
For any industry interested in technology licensing, platform integration or custom components
Create market leading products for your customers
For labs and healthcare systems requiring unique solutions
Bespoke product development tailored to your specific needs
For diagnostic companies, including veterinary
Specialised assay development fit for your purpose
For biotechs and pharma companies
Develop commercial CDx, complementary diagnostics or tools for clinical trials and research


Proven Partnership Success
We've collaborated with industry leaders to deliver breakthrough multiplexed solutions. From adapting our assays for the GeneXpert® platforms used globally, to out-licensing for oncology applications, these partnerships demonstrate our ability to deliver complex solutions at commercial scale.

Cepheid
Collaboration
Adapting SpeeDx assays
for the GeneXpert®
platform

BioCartis
Technology
Out-licensing
of PlexZyme® and PlexPrime®
for oncology applications

GSK
Development
Joint development
of novel
diagnostic solutions

Labcorp
Partnership
Bringing SpeeDx
technology to the largest
US reference lab network
Partnership Advantage | What This Means For You |
|---|---|
Guideline-Influencing Technology | Our ResistancePlus® tests have impacted CDC, BASHH, IUSTI, HAS, KDCA and Australian STI treatment guidelines, providing clinical credbility for your laboratory services |
Platform Flexibility | Expertise validating PCR platforms from suppliers such as Roche, Thermo Fisher Applied Biosystems, Bio-Rad, and Cepheid. We can implement assays on your existing instrumentation |
Accelerated Timelines | Proprietary technology platforms and assay development experience enable accelerated product development cycles, providing a fast track for your multiplexed development |
Regulatory Expertise | Navigated submissions across multiple product lines with IVDR, TGA, and Health Canada |
Proven Commercial Scale | Active in 100+ laboratories across 30+ countries, processing hundreds of thousands of patient samples annually |
Let's Create Your Ideal Solution
Tell us about your needs and we'll design the right partnership approach:
Co-Development
Not
Sure?
"I'd like to discuss options"
Find The Option That Fits
Every product development journey is unique. Schedule a consultation with our partnership team to discuss your specific requirements, timeline, and commercial objectives.
We'll design a collaboration approach tailored to your strategic goals.
CUSTOM DEVELOPMENT
Our proven four-stage development framework ensures predictable timelines, controlled costs, and successful outcomes. Unlike traditional development approaches that can take years, SpeeDx's integrated expertise and proprietary technology platforms typically reduce development timelines by 40% compared to industry standards.
Each project begins with a thorough discovery phase where we assess technical feasibility, define clinical requirements, and establish clear success criteria. Our experienced team then executes development with regular milestone reviews, ensuring you maintain full visibility and control throughout the process.
We've successfully delivered custom diagnostic solutions for global pharmaceutical companies, diagnostic manufacturers, and healthcare systems—from rapid COVID-19 response assays to complex STI resistance panels. Our flexible engagement models accommodate your specific needs, whether you require complete turnkey development or targeted support for specific development stages
*For research use only. Not for use in diagnostic procedures.
Discovery & Design
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Requirements gathering
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Feasibility assessment
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Target selection
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Project planning
Development & Optimization
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Assay development
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Multiplexing optimization
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Regulatory documentation
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Quality system integration
Validation & Verification
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Clinical sample testing
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Performance validation
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Ongoing technical support
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Continuous improvement
Launch & Support
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Manufacturing scale-up
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Commercial launch support
