PriMERx®: Revolutionizing Personalized Medicine with Automated Pharmacogenetic Interpretation
Transforming patient care with precision prescribing, powered by genetic insights. PriMERx® delivers actionable pharmacogenetic guidance directly to clinicians.
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Unlocking Precision Prescribing: Why Pharmacogenetics Matters Today
Over 60% of patients do not respond optimally to standard drug therapies. Genetic differences significantly influence how individuals metabolize and respond to medications, leading to varied treatment outcomes and potential side effects.
Adverse drug reactions (ADRs) cause significant morbidity and healthcare costs. Pharmacogenetic (PGx) testing can reduce these by tailoring prescriptions to individual genetic profiles, enhancing safety and efficacy.
Despite proven benefits, PGx testing remains underutilized due to complexity in interpretation and inconsistent clinical guidelines. PriMERx® addresses these challenges directly.
Meet PriMERx®: Your Clinical Partner for Automated PGx Interpretation
Automated Interpretation
PriMERx® automates complex genetic test result interpretation, translating raw genetic data into clear, actionable prescribing recommendations for medical practitioners.
Seamless Workflow
PriMERx® integrates into existing clinical workflows, reducing turnaround time and minimizing human error.
Evidence-Based Guidance
Powered by the latest evidence from CPIC, DPWD and drug labeling, ensuring up-to-date, trustworthy recommendations.
The Science Behind PriMERx®: Evidence-Based and Comprehensive
PriMERx® supports the interpretation of over 35 key pharmacogenes, covering diverse drug classes including cardiovascular medications, psychiatric drugs, oncology treatments, and analgesics.
The system incorporates rare and ethnicity-specific genetic variants to provide accurate and equitable recommendations for all patient populations, ensuring inclusive care.
PriMERx aligns strictly with Clinical Pharmacogenetics Implementation Consortium (CPIC) guidelines and Dutch Pharmacogenetics Working Group (DPWD), guaranteeing clinical validity and reliability.
How PriMERx® Works: From Genetic Data to Clinical Decision Support
Real-World Impact: Improving Patient Outcomes and Provider Confidence
Optimized Care
Enables clinicians to avoid trial-and-error prescribing, significantly reducing adverse drug reactions and hospitalizations by tailoring therapies.
Empowered Patients
Supports informed consent and patient education by providing clear, understandable genetic insights, fostering better patient engagement.
Confident Prescribing
Empowers pharmacists and prescribers with the confidence to implement precision medicine effectively in routine care, enhancing clinical decisions.
Services Offered by PriMERx®
Array Design
Develops custom genetic arrays tailored to specific research or clinical needs, ensuring relevant variant coverage for precise pharmacogenetic insights.
Local Population Adaptation
Adjusts pharmacogenetic recommendations to reflect the unique genetic profiles and healthcare contexts of diverse local populations, optimizing treatment efficacy.
Multilingual Recommendations
Provides pharmacogenetic recommendations translated into local languages, enhancing comprehension and clinical applicability for healthcare providers globally.
Seamless Integration & Support: Designed for Your Practice
Universal Compatibility
PriMERx® is compatible with diverse laboratory data formats, ensuring smooth data analysis.
Continuous Updates
Our system receives ongoing updates to ensure it reflects the latest scientific discoveries and regulatory changes in pharmacogenetics.
Dedicated Support
We provide comprehensive training, efficient troubleshooting, and personalized onboarding to get your practice started.
Join the Precision Medicine Revolution with PriMERx®
Empower your practice with automated, evidence-based pharmacogenetic interpretation. Improve patient safety, optimize therapy outcomes, and significantly reduce healthcare costs.
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