PreciseEHR

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What is PreciseEHR?

PreciseEHR is our secure, digital health platform designed to deliver your pharmacogenomics and nutrigenomics test results directly to your fingertips. Built for both patients and healthcare providers, PreciseEHR transforms your DNA report into an easy-to-understand, actionable experience.

No more bulky paperwork or waiting for courier delivery.

Your report is ready as soon as it’s processed digitally delivered through PreciseEHR.

BENEFITS OF PRECISE EHR

Why use PreciseEHR

Your Genetic Blueprint, Just A Tap Away.

Instant Access

View your report anytime, anywhere via mobile or desktop

Data Security

End-to-end encryption and medical-grade privacy

User-Friendly Design

Easy to navigate, even if you're not tech-savvy

Doctor-Ready Format

Shareable with your physician for clinical decision-making

Lifetime Storage

Your data stays with you—forever

COMPREHENSIVE REPORT

Clinical-Grade Decision Support

PreciseEHR is built with physicians in mind. The report is comprehensive, covers:

  • Full drug-gene interaction tables
  • Clinical annotations and references
  • Clear summary for prescribing decisions
Precise PGx and NGx report

EASY-TO-FOLLOW GUIDE

Get Started with PreciseEHR

Unlock the full potential of the PreciseEHR app with this easy-to-follow guide, covering everything from installation and account verification to navigating the platform.

Need A Printed Report?

While we encourage digital access for efficiency and environmental sustainability, your report can be downloaded from PreciseEHR app for your own printing. If you prefer an official printed hardcopy report, it is available upon request. Contact our authorized healthcare partner to request a hardcopy (additional fee applies).

SUPPORT & TROUBLESHOOTING

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Frequently Asked Questions

What is the difference between DNA testing and Pharmacogenomics?

DNA testing, or genetic testing, comes in many forms, including tests for ancestry, relationships, inherited diseases, cancer risks, and medical diagnoses. These tests analyze your genes to detect genetic conditions, assess disease risk, or determine hereditary traits.

Pharmacogenomics (PGx), on the other hand, focuses specifically on how your genes affect your response to medications. It helps healthcare professionals personalize treatment plans, minimize the risk of adverse drug reactions, optimize drug effectiveness and dosing.

While genetic testing can help identify potential health risks, PRECISE Pharmacogenomics (PGx) is a clinical-accredited medication genetic test that helps ensure your medications are tailored specifically for you — enhancing safety and treatment effectiveness.

Is PRECISE Pharmacogenomics reliable?

Yes. PRECISE Pharmacogenomics (PGx) provides comprehensive genome-wide coverage, analyzing nearly 100,000 ADME markers and over 1,000 genes, covering more than 500 commonly used medications across 20+ therapeutic areas, including:

  • Painkillers
  • Antibiotics
  • Diabetes medications
  • Heart disease treatments
  • Cancer therapies

Awarded as “The First Clinical Recommended Genome-Wide Pharmacogenomics” by the Malaysia Book of Records (MBR). This report does not replace a medical consultation with your doctor. Please consult your treating medical doctor if medication changes is required.

How accurate is PRECISE Pharmacogenomics?

PRECISE Pharmacogenomics (PGx) boasts an analytical accuracy of over 99%, making it one of the most precise and reliable pharmacogenomics test available. Our platform is backed by:

  • CAP & ISO 15189 laboratory compliance for highest-quality standards
  • HSA (Health Sciences Authority, Singapore) – Clinical Recommendation of Targeted Treatment
  • UKAS (United Kingdom Accreditation Service) – NQA (National Quality Assurance Limited) assessed and ISO13485:2016 accredited
Who should consider getting a PRECISE Pharmacogenomics test?

PRECISE Pharmacogenomics test is beneficial for anyone who takes medications or wants a personalized approach to treatment. It is especially recommended for:

  • Individuals on long-term medications (e.g., hypertension, diabetes, mental health conditions)
  • Those with a history or family history of adverse drug reactions (ADRs)
  • Patients undergoing chemotherapy or chronic disease treatments 
  • Individuals who want to optimize medication effectiveness and safety
  • Proactive individuals who want a “genomic insurance” test before any medication is needed
Can children or elderly individuals take the PRECISE Pharmacogenomics test?

Yes! PRECISE Pharmacogenomics testing is suitable for all ages and can be especially beneficial for:

  • Children – Helps identify potential drug responses early, ensuring safer and more effective treatments as they grow.
  • Elderly individuals – Particularly useful in managing multiple medications, reducing the risk of medication side effects and ensures medications are tailored for safer use.

While a child’s genetic profile remains the same for life, medication dosages may need adjustments as they grow. This test is done once and can be used for a lifetime.

Does my pharmacogenomics result change over time?

No. Your genetic makeup does not change over time, meaning your PRECISE Pharmacogenomics results remain valid for life. Test once, use it for life. However, as new medications and research emerge, updates may be available to enhance treatment recommendations.