Pharmacogenomics Technology

Global Pharmacogenomics Technology Market to Reach US$11.4 Billion by 2030

The global market for Pharmacogenomics Technology estimated at US$7.1 Billion in the year 2024, is expected to reach US$11.4 Billion by 2030, growing at a CAGR of 8.2% over the analysis period 2024-2030. Oncology, one of the segments analyzed in the report, is expected to record a 9.4% CAGR and reach US$5.3 Billion by the end of the analysis period. Growth in the Neurological Disorders segment is estimated at 8.9% CAGR over the analysis period.

The U.S. Market is Estimated at US$1.9 Billion While China is Forecast to Grow at 12.9% CAGR

The Pharmacogenomics Technology market in the U.S. is estimated at US$1.9 Billion in the year 2024. China, the world`s second largest economy, is forecast to reach a projected market size of US$2.5 Billion by the year 2030 trailing a CAGR of 12.9% over the analysis period 2024-2030. Among the other noteworthy geographic markets are Japan and Canada, each forecast to grow at a CAGR of 4.1% and 7.9% respectively over the analysis period. Within Europe, Germany is forecast to grow at approximately 5.4% CAGR.

Pharmacogenomics Technology Market: Key Trends & Drivers Summarized

How Is Pharmacogenomics Transforming Drug Development and Personalized Medicine?

Pharmacogenomics technology is revolutionizing the pharmaceutical industry by enabling personalized medicine based on an individual’s genetic makeup. By studying how genetic variations influence drug response, pharmacogenomics allows for the development of targeted therapies, optimized drug dosages, and reduced adverse reactions. This shift from a one-size-fits-all approach to precision medicine enhances treatment efficacy and minimizes trial-and-error prescribing, significantly improving patient outcomes.

Regulatory agencies such as the U.S. Food and Drug Administration (FDA), European Medicines Agency (EMA), and the International Council for Harmonisation (ICH) are increasingly recognizing pharmacogenomics in drug approvals, labeling, and post-market surveillance. Many pharmaceutical companies are integrating pharmacogenomic data into clinical trials to identify biomarkers, stratify patient populations, and accelerate drug development timelines. With the rapid advancement of next-generation sequencing (NGS), CRISPR-based gene editing, and artificial intelligence (AI)-powered genetic analysis, pharmacogenomics is poised to become a cornerstone of precision medicine.

What Are the Key Trends Driving the Growth of Pharmacogenomics Technology?

The field of pharmacogenomics is evolving rapidly, driven by breakthroughs in genomic sequencing, bioinformatics, and AI-driven drug discovery. One of the most significant trends is the widespread adoption of whole-genome sequencing (WGS) and next-generation sequencing (NGS), which enable rapid and cost-effective identification of genetic variants linked to drug metabolism. With the decreasing cost of sequencing technologies, pharmacogenomics testing is becoming more accessible for clinical applications and population-wide studies.

Another key trend is the integration of AI and machine learning (ML) in pharmacogenomics research. AI-powered algorithms can analyze vast amounts of genetic data to identify drug-gene interactions, predict treatment responses, and develop personalized drug regimens. AI-driven drug discovery platforms are also accelerating the identification of novel biomarkers and therapeutic targets, reducing the time and cost associated with traditional drug development.

The rise of direct-to-consumer (DTC) pharmacogenomics testing is another transformative trend. Companies like 23andMe and Color Genomics are offering genetic testing kits that provide consumers with insights into their drug metabolism and potential adverse drug reactions. While regulatory oversight remains a challenge, the increasing demand for consumer-driven healthcare is fueling the growth of this market.

Furthermore, CRISPR-based gene editing and gene therapy advancements are expanding the scope of pharmacogenomics beyond diagnostics into therapeutic applications. Gene-editing technologies are enabling customized drug development, targeted cancer therapies, and rare disease treatments, further propelling the demand for pharmacogenomics-driven precision medicine.

How Are End-Use Applications Shaping the Pharmacogenomics Market?

Pharmacogenomics technology is influencing multiple therapeutic areas, including oncology, cardiology, psychiatry, neurology, and infectious diseases. Each segment benefits from pharmacogenomics in unique ways, optimizing drug selection and treatment strategies.

Oncology is one of the most significant areas where pharmacogenomics is making an impact. Targeted cancer therapies such as HER2 inhibitors for breast cancer (trastuzumab) and EGFR inhibitors for lung cancer (gefitinib) are based on genetic profiling. Pharmacogenomic testing helps oncologists determine which patients will benefit most from specific treatments, reducing toxicity and improving survival rates. The rise of companion diagnostics, which pair genetic testing with specific cancer drugs, is further driving growth in this sector.

In cardiology, pharmacogenomics is being used to tailor treatments for hypertension, anticoagulation, and cholesterol management. Genetic testing can predict how patients metabolize clopidogrel (Plavix), warfarin, and statins, ensuring that they receive the most effective and safest dosage. This reduces the risk of adverse drug reactions (ADRs) and thrombotic complications, improving cardiovascular disease management.

Psychiatry and neurology are also experiencing significant advancements due to pharmacogenomics. Antidepressants, antipsychotics, and epilepsy medications often exhibit high variability in patient response. Genetic testing helps predict how individuals metabolize drugs such as SSRIs, lithium, and carbamazepine, reducing treatment resistance and side effects. Pharmacogenomics is also playing a role in Alzheimer’s and Parkinson’s disease research, helping to identify potential therapeutic targets based on genetic risk factors.

In the infectious disease sector, pharmacogenomics is being applied to antiviral therapies, antibiotic resistance studies, and vaccine development. For example, genetic testing can determine how patients respond to HIV treatments like abacavir (HLA-B*5701 screening) or hepatitis C therapies, improving antiviral efficacy and reducing hypersensitivity reactions.

Additionally, pharmacogenomics is playing a crucial role in rare disease drug development and orphan drug approvals. Many genetic disorders require highly targeted therapies, and pharmacogenomics is enabling the identification of gene-based treatment strategies for conditions like cystic fibrosis, sickle cell disease, and Duchenne muscular dystrophy.

What Factors Are Driving the Growth of the Pharmacogenomics Technology Market?

The growth in the pharmacogenomics technology market is driven by several factors, including advancements in genomic sequencing, increasing demand for personalized medicine, regulatory support, and expanding applications in drug development. As healthcare shifts toward precision medicine, pharmaceutical companies, research institutions, and healthcare providers are investing heavily in genetic testing, bioinformatics platforms, and AI-driven drug discovery tools.

One of the primary growth drivers is the decreasing cost of genetic sequencing. The cost of whole-genome sequencing has dropped significantly, making pharmacogenomics testing more accessible and cost-effective. As a result, healthcare providers are incorporating genetic profiling into routine clinical practice, expanding the market for pharmacogenomics-based diagnostics and therapeutics.

Regulatory agencies are also playing a key role in promoting pharmacogenomics. The FDA has issued pharmacogenomic labeling for over 300 drugs, highlighting genetic markers that influence drug metabolism and efficacy. Additionally, initiatives such as the All of Us Research Program (U.S.) and the UK Biobank Project are collecting large-scale genetic data to advance pharmacogenomics research, fueling further adoption of the technology.

The increasing prevalence of chronic diseases, cancer, and drug-resistant infections is also driving demand for pharmacogenomics solutions. As traditional treatment approaches often result in variable drug responses and adverse reactions, pharmacogenomics provides a solution by enabling precision prescribing and individualized treatment strategies. Furthermore, pharmaceutical companies are leveraging pharmacogenomics to optimize clinical trials and accelerate drug development. By stratifying patient populations based on genetic profiles, companies can improve trial success rates, reduce drug development costs, and bring therapies to market faster. The rise of companion diagnostics and biomarker-driven drug approvals is further strengthening the link between pharmacogenomics and pharmaceutical innovation.

Additionally, government funding and public-private partnerships are fueling research and commercialization efforts. Organizations such as the National Institutes of Health (NIH), the European Medicines Agency (EMA), and the Japan Agency for Medical Research and Development (AMED) are investing in pharmacogenomics research, enabling breakthroughs in gene-based therapy development and population-wide genetic screening initiatives. As pharmacogenomics continues to integrate with AI, big data, and precision drug discovery, the field is poised for exponential growth, transforming the way drugs are developed, prescribed, and monitored. With advancements in gene sequencing, biomarker identification, and AI-driven analysis, pharmacogenomics will play an increasingly central role in shaping the future of personalized medicine and precision healthcare.

SCOPE OF STUDY:

The report analyzes the Pharmacogenomics Technology market in terms of units by the following Segments, and Geographic Regions/Countries:

Segments:
Therapeutic Area (Oncology, Neurological Disorders, Cardiovascular Disease, Immunological Disorders, Infectious Diseases); Technology (PCR, In-situ Hybridization, Immunohistochemistry, Sequencing, Others)

Geographic Regions/Countries:
World; United States; Canada; Japan; China; Europe (France; Germany; Italy; United Kingdom; Spain; Russia; and Rest of Europe); Asia-Pacific (Australia; India; South Korea; and Rest of Asia-Pacific); Latin America (Argentina; Brazil; Mexico; and Rest of Latin America); Middle East (Iran; Israel; Saudi Arabia; United Arab Emirates; and Rest of Middle East); and Africa.

Select Competitors (Total 42 Featured) -

• 23andMe, Inc.
• Abbott Laboratories
• Agilent Technologies, Inc.
• Becton, Dickinson and Company
• bioMérieux S.A.
• Bio-Rad Laboratories, Inc.
• Coriell Life Sciences
• Eurofins Scientific
• F. Hoffmann-La Roche Ltd
• Genomind, Inc.
• Guardant Health, Inc.
• Illumina, Inc.
• Merck KGaA
• Myriad Genetics, Inc.
• Pacific Biosciences of California, Inc.
• Pathway Genomics Corporation
• PerkinElmer, Inc.
• QIAGEN N.V.
• Thermo Fisher Scientific Inc.
• Wellness Labs

TARIFF IMPACT FACTOR

Our new release incorporates impact of tariffs on geographical markets as we predict a shift in competitiveness of companies based on HQ country, manufacturing base, exports and imports (finished goods and OEM). This intricate and multifaceted market reality will impact competitors by artificially increasing the COGS, reducing profitability, reconfiguring supply chains, amongst other micro and macro market dynamics.

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APRIL 2025: NEGOTIATION PHASE

Our April release addresses the impact of tariffs on the overall global market and presents market adjustments by geography. Our trajectories are based on historic data and evolving market impacting factors.

JULY 2025 FINAL TARIFF RESET

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