We help make risk actionable with industry-leading risk assessment and prevention platform.
Nala CDS integrates AI-powered tools to improve diagnostic yield and reduce turnaround time. With customizable protocols for panels, exomes, and genomes, Nala CDS simplifies complex bioinformatics workflows while maintaining full transparency and control. Its comprehensive annotation engine supports all sequencing input types, automating the entire diagnostic process from sequencing to actionable insights.
Our flagship PGx module, RxMax™, is a comprehensive solution covering 35 pharmacogenes and over 300 clinically actionable gene-drug interactions, spanning 15 therapeutic areas, including cardiology, oncology, psychiatry, infectious disease, and more.
Nala Clinical Decision Support (CDS) houses 10+ polygenic risk scores for complex conditions in cancer, cardiometabolic, and neurodegenerative conditions. All algorithms are normalization based on diverse population data sets.
Nala CDS houses combined risk scoring using genetics, epigenetics, and clinical risk scores to increase accuracy and actionability for prevention of complex conditions.
Support early diagnosis and carrier screening with panels aligned to ACMG guidelines, covering a wide range of inherited conditions. Our curated pipeline ensures accurate classification, clinical relevance, and compatibility with confirmatory workflows.
Explore traits related to nutrition, metabolism, skin health, and lifestyle through polygenic and trait-based insights— designed to support preventive care and optimize long-term health strategies.
From early research to clinical deployment, our solutions span key disease areas— pharmacogenomics, cancer, and chronic conditions—designed to support labs and research teams through every phase of development and regulation.
Support high-volume testing and population studies with a secure, scalable reporting system—discover how it works in Nala CDS demo video.
Gain instant access to 10+ modules covering pharmacogenomics, polygenic risk scoring, rare disease, and more—all under a single license. Compatible with qPCR, microarrays, WGS, and WES.
Manage every step from collection to report with a secure platform that offers audit trails, role-based access, and real-time tracking—ideal for national programs and institutional labs.
Seamlessly connect genomic reports to clinical workflows with HL7-based APIs. Reduce friction for hospital IT teams while improving turnaround time and physician usability.
Adapt report design, branding, and delivery formats to match your lab’s protocol or research needs. Choose secure cloud, on-premise, or offline deployments to meet your data governance requirements.
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Meet with our team to discuss your goals—whether clinical testing or research.
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Complete a short KYC form and receive a customized plan—covering lab setup, study design, or platform selection.
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Create experiment plan for six months and design customization with the team for full scale deployment.
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Receive clear reports and ready-to-use data, with ongoing training and collaboration for labs or research teams.
Tell us your goals in lab, clinical, or research projects and we’ll help you take the next step
