The processes that activate and eliminate medications, is shaped by each person’s unique genetic makeup, especially the genes coding for cytochrome P450 (CYP450) enzymes.

These enzymes are the key drivers in metabolizing nearly 80% of drugs on the market, meaning genetic differences can dramatically influence how patients respond to treatment.

Understanding these variations allows healthcare professionals and laboratories to optimise dosing, improve efficacy, and reduce the risk of adverse reactions, bringing the promise of personalised medicine closer to everyday practice

At Mathgen, we help diagnostic laboratories and healthcare teams harness the power of pharmacogenetics to deliver truly personalised patient care.

Our consulting services guide laboratories through the implementation of pharmacogenetic testing, from assay development and technology integration to quality control. We also provide expert support in interpreting pharmacogenetic results and translating them into actionable insights that clinicians can use to optimise therapy decisions.

By combining scientific rigor, advanced analytics, and practical guidance, we empower your team to transform complex pharmacogenetic data into reliable, clinically relevant information, turning pharmacogenetics from a research tool into a routine part of patient care.

With over a decade of experience leading diagnostic laboratory specialised in pharmacogenetics, we combine scientific expertise and practical know-how to deliver high-impact solutions.

Our experience spans the full spectrum of pharmacogenetic testing, including designing and validating assays, interpreting complex genetic data, and training medical professionals to apply these insights in clinical practice.

We also provide expertise for: