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FOR LABORATORIES
Expand your laboratory capabilities with human genomic offerings​

 

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High-quality offerings with certified products
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NalaGenetics specializes in genomics for highly inherited conditions, from lab setup to reporting
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20+

lab setup

200,000+

report generated

<3 Months

from set up to launch

We have helped design, build, operate, and scale labs across Southeast Asia. Partner with us for human genomic solutions.

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9.7

It was a great experience working with Focus theme. We highly recommend it! Far far away, behind the word mountains, far from the countries Vokalia.

Walter Craftson, Acme
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8.5

Far far away, behind the word mountains, far from the countries Vokalia and Consonantia, there live the blind texts. It was a great experience working with Focus theme.

Cole Sullivan
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9.6

It was a great experience working with Focus theme. We highly recommend it! Far far away, behind the word mountains, far from the countries Vokalia.

Margaret Fitch, Acme
Nala Clinical Decision Support™

An end-to-end support software for every laboratory handling genetic samples

Nala Clinical Decision Support™ (CDS) is a genetic interpretation software trademarked by NalaGenetics, built to ISO standards for product development quality, security, and confidentiality.

Genetic interpretations for:
 Personalised Medication​
Personalised Diet and Nutrition​
Personalised Lifestyle​
Breast Cancer Screening

Our milestone with Nala Clinical Decision Support™

12+

Countries

10+

Report Modules

1000+

Reports Generated

20+

Hospital Labs
Nala PGx Core®

Plug-and-play pharmacogenomics solution on real-time qPCR technology

  • Nala PGx Core® is a multi-gene panel test designed to analyze four important pharmacogenes (CYP2C9, CYP2C19, CYP2D6 and SLCO1B1).​
  • Nala PGx Core® utilizes the real-time qPCR method to ensure that the results are accurate and reliable with a shorter turnaround time.
  • Genetic interpretation of results is available when used with Nala CDS software.

Our panel has been validated and run in clinical labs around the world

≥96.9%

Concordance

Variant-level concordance resulting in a diplotype-level concordance of ≥ 94.7%

>97% ​

Sensitivity and Specificity

97% in CYP2D6, and 100% in the rest of the genes

100%

Precision Rate

In both intra- and inter-precision studies
Our solutions are used and recognized globally​
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Nalagenetics Launches Brand New Breast Cancer Risk Prediction Test: MammoReady

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Nalagenetics Launches Brand New Breast Cancer Risk Prediction Test: MammoReady

Your privacy is our top priority
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Your Privacy, Your Control

We take data privacy seriously. Your genetic information is exclusively yours, and we won't share it with anyone outside NalaGenetics without your consent. You're in charge of deciding who sees your data and how it's utilized.

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Encrypted Security Shield

Think of your genetic data as a fortress guarded by the best security tech. We adhere to ISO-27001 standard to ensure its safety. It's encrypted and regularly checked for any weak spots to ensure your data stays safe from cyber threats.

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Contributing to Research, Safely

Getting tested with NalaGenetics gives you the option to contribute to our research. If you allow us to use it for research, we make your data anonymous unless you choose otherwise. We remove anything that could identify you, ensuring your privacy. It's like contributing to a greater cause without compromising your personal fortress.

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