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Awarded by the malaysia book of records

Precision Diagnostics being the “1ˢᵗ Clinical Recommended for Genome-Wide Pharmacogenomics since 2023”

Malaysian Book of Records for Precision Diagnostics

Our Collaborators & Partners

DNA is the future

Through DNA, identifying the best course of treatment, ensures that interventions are not just generic but specifically suited to their genetic profile.

Tailor Treatments

GPs and Pharmacists can recommend the precise treatment and medication from the start without relying on a “one-size-fits-all” approach

Lifetime Value

Roughly RM2+ per gene, the PRECISE Pharmacogenomics test offers more than >1,000 genes, providing personalised insights at an exceptional price

Become a Partner

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Picture of PRECISE Pharmacogenomics Buccal Swab box

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Become a Research Collaborator

Our team at Precision Diagnostics will carefully review the following queries. Our scientific collaborations empower the development of groundbreaking tools and technologies that push the boundaries of discovery to Advancing Tomorrow's Cures.

Research Form

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How to use DNA Collection Kit?

Click here and follow the instructions! Once finished, place the sample in the hazard bag and return to your respective PIC (person-in-charge).

What is Pharmacogenomics (PGx)?

Pharmacogenomics (PGx), a core component in Precision Medicine, is the study of how genes affect a person’s response to medications. This field combines pharmacology (the science of drugs) and genomics (the study of genes and their functions) to develop effective, safe medications that can be prescribed based on a person’s genetic makeup while preventing medications’ side effects (known as Adverse Drug Reactions, ADRs). In other words, a medication can be safe for one but harmful for the other, even when prescribed with similar doses.

This test is open to the general public.
While there are no age restrictions for Pharmacogenomic (PGx) tests. For individuals below the age of 18, a legal guardian must complete the request and consent form. In the case of children, their phenotype (DNA traits) remains the same, but medication doses might change as they grow.

How accurate is PRECISE Pharmacogenomics?

With an analytical accuracy and reliability of over 99%, our genome-wide platform has proven to be highly precise and dependable. The clinical recommendations in our report are accredited by the Health Science Authority (HSA) of Singapore – HSA Class A Medical Device, NQA (National Quality Assurance Limited) accredited by UKAS (United Kingdom Accreditation Service) for ISO13485 certified; while our laboratory operations strictly adhere to the standards set by CAP and ISO 15189.

ATCC, known as Advancing Tomorrow’s Cure Community, is a community established by Beacon Hospital to study how Asian genetics react to current medicines. To enjoy the sponsored pricing, it is REQUIRED to partake in the ATCC consent.

Your deidentified sample will be stored indefinitely as anonymous specimens for the option of being able to update your report at the minimal cost after the first FOC update with joining the ATCC, as well as for research purposes. Only an identification specimen number will be used, ensuring the anonymity and privacy of your data.
As for the possibility of research direction changes leading to activities related to cloning, Malaysia does not support human cloning therefore we will not be embarking on this area of research. Pharmacogenomics primarily focuses on understanding how an individual’s genetic makeup influences their response to drugs, optimising drug therapy based on genetic factors, and advancing personalized medicine. While research directions can evolve over time, the core focus of pharmacogenomics remains centered on drug response and genetic variability rather than cloning or genetic manipulation for other purposes.

Frequently Asked Questions

In Malaysia, the rising prevalence of chronic diseases like diabetes, heart disease, and cancer is a growing concern. Many Malaysians are battling these severe conditions daily, often relying on medications that may not work optimally for everyone. But what if there was a way to tailor your treatment to your unique genetic makeup?