Overview
Clinical Decision Support - Dashboard Overview
Overview of reports and order statuses in a single, intuitive dashboard for streamlined clinical workflows.
Clinical Decision Support - Dashboard Overview
Clinical Decision Support - Launch Analysis
Clinical Decision Support - Reports

NalaGenetics - Capabilities Overview
NalaGenetics Clinical Decision Support (CDS) is a secure, ISO-aligned software platform that delivers genetic insights directly into clinical and research workflows. We report ACMG P/LP variants, polygenic risk scores, pharmacogenomics results, and more.
Our capabilities include:
- Co-develop: exploring new algorithms based on new data sets and guidelines
- Enhance: improving existing algorithms through localization, normalization, and integration of multi-omics data (e.g., clinical, methylation)
- Implement: designing and customizing clinical-grade reports and patient interfaces, including mobile access and integration into electronic health records
CDS is built for a wide range of organizations, including hospitals, diagnostic laboratories, research institutions, and digital health providers that seek to integrate genetic data into their workflows. The platform simplifies complex data interpretation through an intuitive interface and supports seamless integration with major EHR systems.
Trusted by more than 20 laboratories and hospitals across 12 countries, CDS has generated over 40,000 reports to date. With more than 10 configurable report modules, the platform is adaptable for clinical delivery, translational research, and population health initiatives, making it a powerful solution for personalized care at scale.
For teams aiming to bridge the gap between genetic science and real-world implementation, CDS provides a secure and efficient foundation to scale precision medicine and enable collaborative innovation.
Highlights
- Platform agnostic and standards-driven: compatible with qPCR, microarray, short-read and long-read sequencing data, and designed to integrate seamlessly with EHR systems (e.g., EPIC, homegrown) and research environments, following ISO standards for security, quality, and confidentiality.
- Actionable insights for clinicians: translates complex genetic data into clinical-grade reports with clear follow-up actions (alternative medications, preventive interventions), aligned with international guidelines and professional societies in oncology, cardiometabolic, and neurodegenerative diseases.
- Proven flexibility and scalability: offers more than 10 configurable report modules and has been deployed across 12+ countries, 20+ laboratories and hospitals, and 40,000+ reports, in partnership with top providers in Trusted Research Environments and global cloud platforms.
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Pricing
Dimension | Description | Cost/12 months | Overage cost |
---|---|---|---|
Utilization Based | Pay-as-you-go model: billed monthly based on total number of reports generated. Tiered pricing applies depending on usage volume. | $0.00 | - |
Basic License (Annual) | Includes up to 50 reports per month. Additional reports will be charged per usage. | $40,000.00 | |
Pro License (Annual) | Includes up to 100 reports per month with free re-analysis. Additional reports will be charged separately. | $50,000.00 |
The following dimensions are not included in the contract terms, which will be charged based on your usage.
Dimension | Cost/unit |
---|---|
Less than/equal to 50 report | $80.00 |
More than 50 report | $50.00 |
Vendor refund policy
For more information, please contact clinicalstudies@nalagenetics.com or help@nalagenetics.comÂ
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For support and more information, please contact clinicalstudies@nalagenetics.com or help@nalagenetics.comÂ
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