Develop

Advancing precision medicine with next-generation genomics solutions
We strengthen your late-stage research program by developing tailored, validated and scalable NGS-based assays, supporting efficient patient selection across borders.
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Precision genomics for smarter drug development

Effective patient selection for innovative therapies relies on high-quality biomarker testing, yet navigating evolving technologies can be challenging.

With our advanced technology, leading next-generation sequencing (NGS) diagnostic solutions, custom assay services, and global partner ecosystem for regulatory submission, you can pursue the right diagnostic path to maximize patient impact.

Leverage our expertise in developing and deploying genomics applications and the data generated within the SOPHiA GENETICS network to enhance patient and market access to relevant genomic information, and match patients to the right clinical trials and treatments.
*SOPHiA DDMTM Clinical Trial Assay and SOPHiA DMMTM Follow-on Dx can be further validated to Companion Diagnostic (CDx) level

Optimizing diagnostic strategy for program success

Unlock your program with flexible NGS solutions

Advance your research program with reliable and high-performing assays tailored to your biomarker needs. Supported by our technical and scientific experts, we help you build, refine, and launch assays that offer best-in-class analytics for global market implementation.

Whether leveraging existing on-market products or designing new ones, we provide flexible solutions to accelerate your success.
Optimized assays
Develop new NGS-based assays or further enhance our commercially available solutions to meet your unique requirements, with the support from our team of experts.
Cost-effective development
Rely on the tech-agnostic and scalable SOPHiA DDM™ Platform to expedite the development and deployment of highly accurate genomic solutions.
Valuable data
Obtain early real-world data to further validate your solution, gain first adopters’ insights, and drive your commercialization strategy.

Elevate your research with robust clinical trial assays

Design, co-develop, and optimize robust Clinical Trial Assays (CTAs) and algorithms with guidance from technical and scientific experts well-versed in QMS and regulatory requirements at every stage.

Whether building bespoke solutions or leveraging existing assays, we deliver fit-for-purpose solutions that meet regulatory standards, accelerating development success worldwide.
Custom assay design
Benefit from proven expertise in designing, developing, and optimizing NGS-based assays that can be further enhanced and validated.
Streamlined validation
Accelerate your program with adequate validation, and fast and robust assay deployment at your CRO of choice for clinical trial enrollment.
Optimized enrollment
Gain efficiency and flexibility with SOPHiA DDM™ CTA, enabling global clinical trial screening, patient selection, enrollment, and stratification.

Transform drug development with comprehensive CDx

Accelerate market access and optimize resources by co-developing robust end-to-end NGS-based Companion Diagnostics (CDx) solutions tailored to your specific needs.

Combining proprietary NGS assays, advanced analytics, and our hybrid validation and deployment approach, we guide you from design to regulatory approval and commercialization. Achieve efficiency and compliance, while bringing life-changing therapies to patients sooner.
Efficient validation
Achieve efficient, robust analytical validation and select between prospective or retrospective clinical validation, optimized for your unique CDx requirements.
Flexible go-to-market
Optimize CDx development with our hybrid, centralized and decentralized model, ensuring regulatory alignment, smoother approval and rapid commercialization.
Global implementation
Harness the power of the SOPHiA DDM™ global network to upscale local deployment and maximize the decentralization of your newly developed CDx.

“Through this collaboration, we aim to enable the widespread application of precision medicine in oncology across Africa, and thus contributing to the improvement of patient outcomes across the African continent.

“Our collaboration with SOPHiA GENETICS has the potential to uncover genomic mutations that correlate with clinical response to ADCT-402. We have observed significant single-agent clinical activity in our pivotal Phase II trial of ADCT-402 in a broad population of patients with relapsed or refractory diffuse large B-cell lymphoma. The insights from this collaboration will allow us to better identify and understand the characteristics of patients who respond best to treatment. We look forward for the results of this research enabled by SOPHiA’s unique platform”
Patrick van Berkel
Sr VP of Research and Development, ADC Therapeutics

Our Partner Testimonials

A hybrid CDx model in action

SOPHiA GENETICS partners with leading diagnostics companies in key markets to transform how CDx are developed and deployed.

By combining local regulatory expertise and traditional CDx pathways with a universal and scalable platform, we expand the global reach of precision medicine.

SOPHiA GENETICS products are for Research Use Only and not for use in diagnostic procedures unless specified otherwise.

SOPHiA DDM™ Dx Hereditary Cancer Solution, SOPHiA DDM™ Dx RNAtarget Oncology Solution and SOPHiA DDM™ Dx Homologous Recombination Deficiency Solution are available as CE-IVD products for In Vitro Diagnostic Use in the European Economic Area (EEA), the United Kingdom and Switzerland. SOPHiA DDM™ Dx Myeloid Solution and SOPHiA DDM™ Dx Solid Tumor Solution are available as CE-IVD products for In Vitro Diagnostic Use in the EEA, the United Kingdom, Switzerland, and Israel. Information about products that may or may not be available in different countries and if applicable, may or may not have received approval or market clearance by a governmental regulatory body for different indications for use. Please contact us to obtain the appropriate product information for your country of residence.

All third-party trademarks listed by SOPHiA GENETICS remain the property of their respective owners. Unless specifically identified as such, SOPHiA GENETICS’ use of third-party trademarks does not indicate any relationship, sponsorship, or endorsement between SOPHiA GENETICS and the owners of these trademarks. Any references by SOPHiA GENETICS to third-party trademarks is to identify the corresponding third-party goods and/or services and shall be considered nominative fair use under the trademark law.

SOPHiA DDM™ Overview
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