View your report anytime via PreciseEHR.
PreciseEHR is our secure, digital health platform designed to deliver your pharmacogenomic and nutrigenomic 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.
Your report is ready as soon as it’s processed digitally delivered through PreciseEHR.
Your Genetic Insights, Just A Tap Away.
View your report anytime, anywhere via mobile or desktop
End-to-end encryption and medical-grade privacy
Easy to navigate, even if you're not tech-savvy
Shareable with your physician for clinical decision-making
Your data stays with you—forever
PreciseEHR is built with physicians in mind. The report is comprehensive, covers:
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.
While we encourage digital access for speed and sustainability, we do offer a printed hardcopy report upon request. Contact our agent to request a hardcopy (additional fee applies).
Trouble accessing your report? We’re ready to help.
PreciseEHR is available for free download on:
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, chromosomes, or proteins 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, optimize drug selection and dosage, and reduce the risk of adverse drug reactions (ADRs).
While genetic testing can help identify potential health risks, PRECISE Pharmacogenomics (PGx) ensures that your medications are tailored specifically for you—enhancing safety and treatment effectiveness.
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, including:
Awarded as “The First Clinical Recommended Genome-Wide Pharmacogenomics” by the Malaysia Book of Records (MBR), only certified healthcare professionals can interpret the report and provide clinical recommendations, diagnoses, and treatment plans. However, this report does not replace a medical consultation with your doctor.
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;
Pharmacogenomics testing is beneficial for anyone who takes medications or wants a personalized approach to treatment. It is especially recommended for:
Yes! Pharmacogenomics testing is suitable for all ages and can be especially beneficial for:
While a child’s genetic profile remains the same for life, medication dosages may need adjustments as they grow.
No. Your genetic makeup does not change over time, meaning your pharmacogenomics results remain valid for life. However, as new medications and research emerge, updates may be available to enhance treatment recommendations.