Sold by: NalaGenetics
Deployed on AWS
NalaGenetics Clinical Decision Support (CDS) is a secure, ISO-aligned software platform that integrates genetic insights into clinical workflows. Designed to support clinical decision-making using genomic information, CDS provides actionable recommendations, enhances treatment accuracy, and improves patient outcomes through seamless EHR integration.
Overview
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Clinical Decision Support - Dashboard Overview
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Clinical Decision Support - Launch Analysis
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Clinical Decision Support - Reports
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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.
Details
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Delivery method
Deployed on AWS
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Pricing
Pricing is based on the duration and terms of your contract with the vendor, and additional usage. You pay upfront or in installments according to your contract terms with the vendor. This entitles you to a specified quantity of use for the contract duration. Usage-based pricing is in effect for overages or additional usage not covered in the contract. These charges are applied on top of the contract price. If you choose not to renew or replace your contract before the contract end date, access to your entitlements will expire.
Additional AWS infrastructure costs may apply. Use the AWS Pricing Calculator to estimate your infrastructure costs.
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 |
Dimension | Description | Cost/unit |
|---|---|---|
Per Report (<= 50 reports/month) | Up tp 50 reports per month billed at $80/report | $80.00 |
Per Report (>50 reports/month) | Over 50 reports per month billed at $50/report | $50.00 |
Dimensions summary
This listing bills by genetic report volume, with two structures. The annual licenses commit you for a year. The Basic License (Annual) includes up to 50 reports per month, and the Pro License (Annual) includes up to 100 reports per month with free re-analysis. Both charge extra for reports beyond the included count. The Per Report options charge per report, with separate rates for up to 50 reports per month and for over 50 reports per month. The Utilization Based option bills monthly as pay-as-you-go, applying tiered pricing that varies by your total report volume.
Top-of-mind questions for buyers
A report is a genetic test result generated through the Clinical Decision Support platform. Each test you run for a patient produces one report. Reports are counted monthly, and your billing depends on how many you generate within a given month.
Both annual licenses include a set monthly report count. The Basic License (Annual) includes up to 50 reports per month, and the Pro License (Annual) includes up to 100. Reports beyond those counts are charged separately per report in addition to your annual fee.
The Utilization Based option bills monthly as pay-as-you-go, with tiered pricing that shifts by your total report volume. The Per Report options apply a fixed rate per report, with one rate for up to 50 reports per month and another for over 50.
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Support
Vendor support
For support and more information, please contact clinicalstudies@nalagenetics.com or help@nalagenetics.com
AWS infrastructure support
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