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The India precision medicine market was valued at USD 2.68 Billion in 2025, driven by increasing adoption of genomics-based diagnostics and rising government support for personalized healthcare initiatives across the region. The market is anticipated to grow at a CAGR of 11.80% during the forecast period of 2026-2035, with the values likely to reach USD 8.18 Billion by 2035. The market benefits from expanding healthcare infrastructure and growing demand for targeted therapies. Advancements in AI-driven analytics and the integration of electronic health records are expected to boost adoption in the forecast period, contributing to improved patient outcomes and enhanced treatment efficacy.
Compound Annual Growth Rate
11.8%
Value in USD Billion
2026-2035
Precision medicine is an advanced medical approach that tailors treatment and prevention strategies to individual genetic, environmental, and lifestyle factors. It aims to improve patient outcomes by providing more accurate diagnoses and targeted therapies based on personal variability. The precision medicine market in India is experiencing significant growth due to increasing healthcare digitization, rising chronic disease prevalence, and advancements in genomics and data analytics. Government initiatives and growing investments in biotechnology further support market expansion. The market is poised to grow at a CAGR of 11.80% during the forecast period of 2026–2035, driven by evolving clinical practices and the adoption of personalized healthcare solutions.
Increasing Prevalence of Cancer to Elevate the Market Growth
The rising prevalence of cancer is emerging as a highly significant growth driver in the precision medicine market in India. According to the Indian Council of Medical Research (ICMR), it was estimated that over 1.4 million new cancer cases were diagnosed across India in 2023 alone. This rising cancer burden is driving strong demand for personalized and targeted therapies that enhance treatment efficacy and reduce adverse effects. As a result, the adoption of precision medicine is accelerating across the country, thereby fueling substantial and continuous expansion of the market.
4baseCare launched TARGT Indiegene V2 in September 2026, an upgraded comprehensive genomic profiling test designed to support precision oncology in India. The new version covers 2,206 genes and 299 clinically relevant gene fusions, expanding the genomic scope available for cancer biomarker testing. The platform applies a biology-first approach that maps genomic findings across the Hallmarks of Cancer, helping clinicians interpret molecular alterations in the context of tumour biology. The launch builds on 4baseCare’s experience with Indian tumour genomics and aims to improve the relevance of genomic testing for diverse patient populations. It also strengthens India’s domestic capabilities in advanced cancer profiling and personalised treatment planning.
AstraZeneca India and the Government of Andhra Pradesh initiated an integrated precision oncology ecosystem in July 2026, combining artificial intelligence, next-generation sequencing and advanced genomics within the public healthcare system. The initiative includes an Integrated Genomic Solutions Centre in Amaravati focused on genomic diagnostics and biomarker testing for cancers including lung and breast cancer. AstraZeneca is also facilitating deployment of Qure.ai’s AI-powered chest X-ray technology across selected government healthcare facilities to support earlier identification of high-risk patients. The initiative aims to connect screening, genomic testing, diagnosis and personalised treatment through an integrated care pathway, demonstrating increasing public-private collaboration around precision medicine in India.
Fortis Hospitals Bengaluru launched its Preventive Genomics Clinic in April 2026, expanding the application of genomic medicine from disease treatment towards preventive and risk-based healthcare. The clinic offers advanced genetic testing, genetic counselling and personalised treatment planning based on individual genetic profiles. Its services are intended to support early identification of inherited conditions, improve classification of complex diseases and enable more targeted treatment strategies. The initiative represents growing adoption of genomics within mainstream hospital networks rather than limiting advanced genetic testing to specialist laboratories. By integrating genomic assessment with clinical consultations and counselling, Fortis is also strengthening the infrastructure required to translate genetic information into preventive care and personalised clinical decision-making.
Metropolis Healthcare launched its Centre of Genomics in January 2026 to expand precision diagnostics and genomic research capabilities across India. The centre integrates CAP-accredited genomics laboratories in Mumbai and Delhi NCR with next-generation sequencing, bioinformatics and clinical interpretation capabilities. Metropolis also deployed Illumina’s NovaSeq X Series to increase high-throughput sequencing capacity, with the NovaSeq X Plus capable of generating more than 20,000 whole genomes annually. The centre initially supports applications across oncology, reproductive health, neurology, transplant immunology and rare diseases. Metropolis plans to expand its portfolio to more than 500 advanced genomic tests, strengthening the availability of clinically actionable genomic information for personalised healthcare.
India’s precision medicine ecosystem is increasingly moving towards genomic reference data that reflects the country’s population diversity. The GenomeIndia project has completed whole-genome sequencing for more than 10,000 individuals, while its broader biobank contains over 20,000 samples from 83 populations. Research published in 2026 identified nearly 130 million genetic variants among 9,768 sequenced individuals, including around 44 million variants not previously reported in major global databases. These findings highlight the limitations of relying exclusively on genomic reference datasets developed from predominantly European populations. As India-specific genomic resources expand, pharmaceutical companies, diagnostic providers and research institutions are gaining a stronger foundation for developing disease-risk models, pharmacogenomic applications and targeted therapies suited to Indian populations.
Artificial intelligence is becoming increasingly integrated with genomics to interpret large volumes of genetic and clinical information. In February 2026, the Department of Biotechnology highlighted AI-driven gene sequencing as an important component of India’s transition towards personalised prescriptions and predictive medicine. The government also announced Bio-AI Mulankur hubs to integrate AI-based predictions, laboratory validation and data analytics across genomics diagnostics, biomolecular design and synthetic biology. By July 2026, the government reported that GenomeIndia data was being used with AI and machine-learning tools to support indigenous precision medicine applications. This convergence is encouraging investment in computational biology, genomic interpretation and AI-assisted diagnostics while creating demand for platforms capable of translating complex genomic datasets into clinically useful insights.
Cancer care is becoming a major application area for precision medicine in India as genomic profiling and biomarker testing become more integrated into clinical pathways. Government programmes include the DIAMOnDS initiative, which provides advanced molecular diagnostics to eligible lung and breast cancer patients through 25 centres. In parallel, India has established an AI-enabled medical imaging resource containing more than one million radiology images and 20,000 pathology images for developing precision oncology algorithms. Commercial providers are also expanding comprehensive genomic profiling capabilities for cancer patients. These developments are increasing the role of next-generation sequencing, molecular biomarkers, liquid biopsy and AI-supported pathology in treatment selection. The trend is gradually shifting oncology from broad treatment protocols towards molecularly informed diagnosis and therapy selection.
India’s precision medicine ecosystem is increasingly addressing rare and inherited disorders through genomic testing, newborn screening and targeted therapies. The government’s UMMID initiative has established NIDAN Kendras focused on prenatal testing, newborn screening and genetic counselling for families at risk of genetic disorders. GenomeIndia is also creating a population-specific reference dataset that can support research into disease-associated variants across diverse Indian communities. In June 2026, the government highlighted gene therapy and personalised therapies as emerging areas supported by India’s expanding genomic infrastructure. This is broadening precision medicine beyond oncology into rare diseases, inherited disorders and genetic counselling. Greater availability of genomic testing and counselling is expected to strengthen early diagnosis and improve identification of patients who may benefit from targeted interventions.
India is building a larger national infrastructure to convert genomic information into practical healthcare applications. GenomeIndia has archived whole-genome sequencing data for more than 10,000 individuals at the Indian Biological Data Centre, while the project has also established a biobank containing more than 20,000 biospecimens. The IBDC provides dedicated biological-data repositories and high-performance computing infrastructure for research. Government programmes are increasingly connecting these resources with universities, hospitals, research institutions, start-ups and industry through collaborative projects. This is creating an ecosystem in which population genomics, clinical datasets, AI and laboratory research can be combined to develop diagnostic tools and personalised therapies. The resulting infrastructure is particularly relevant for Indian-specific risk prediction, pharmacogenomics and translational precision healthcare.
The market report offers a detailed analysis of the market based on the following segments:
Market Breakup by Type
Market Breakup by Application
Market Breakup by End User
Market Breakup by Region
Segmentation Based on Application to Witness Substantial Growth
Precision medicines have a wide range of applications across various medical fields, including oncology, neurology, immunology, hematology, respiratory diseases, and others. According to the Indian Council of Medical Research (ICMR), India recorded over 14 lakh new cancer cases in 2023, underscoring the urgent need for targeted treatments. This significant cancer burden positions oncology as the leading application segment within the precision medicine market. The increasing adoption of personalized therapies, driven by advances in genetic testing and molecular diagnostics, further supports oncology’s dominance. Although other segments, such as neurology and immunology, are growing steadily, oncology is expected to remain the primary driver of market growth in India.
The precision medicine market report in India covers North India, East and Central India, West India, and South India. Among these, South India is expected to lead due to its robust healthcare infrastructure and progressive medical initiatives. For instance, in April 2025, SunAct Cancer Institute and Smita Memorial Hospital launched a CAR T-Cell Therapy Centre in Kerala, emphasizing precision oncology, pediatric care, and international clinical trials. This development underscores South India's growing role in advancing affordable, cutting-edge cell and gene therapies.
The key features of the market report comprise patent analysis, funding and investment analysis, and strategic initiatives by the leading players. The major companies in the market are as follows:
Strand Life Sciences, established in 2000 and headquartered in Bangalore, India, is a life sciences technology company specializing in bioinformatics, diagnostics, and clinical research. In April 2024, it entered a strategic partnership with SOPHiA GENETICS to advance precision medicine. The collaboration aimed to integrate Strand’s bioinformatics platforms and curated variant databases with the SOPHiA DDM Platform to enhance genomic analysis and support data-driven healthcare decisions, particularly benefiting patient outcomes in India.
Established in 2012 and headquartered in Hyderabad, MapmyGenome India Ltd., is a key player in the India precision medicine market. The company specializes in personal genomics and preventive health solutions. Its product, Cardiomap, exemplifies its focus on cardiovascular health by assessing genetic predisposition to heart conditions. MapmyGenome integrates genetic insights with lifestyle data to support personalized prevention strategies, advancing precision medicine in India.
Redcliffe Labs is actively contributing to the India precision medicine market through innovative diagnostic solutions. It was established in 2018 and is headquartered in Noida, India. In May 2025, the company launched Femcliffe, India’s first women-centric diagnostic platform. Femcliffe offers tailored diagnostic packages across all stages of a woman’s life, addressing conditions like PCOS, reproductive disorders, and metabolic diseases, with services available nationwide.
Headquartered in Basel, Switzerland, and founded in 1996, Novartis AG is actively engaged in the precision medicine market. The company offers extensive educational and digital resources aimed at enhancing biomarker testing and personalized therapies, particularly in oncology and hematology. Through initiatives such as molecular diagnostics in personalized cancer care and essential elements of biomarker testing, Novartis supports healthcare professionals in delivering targeted, individualized treatments aligned with precision medicine principles.
*Please note that this is only a partial list; the complete list of key players is available in the full report. Additionally, the list of key players can be customized to better suit your needs.*
Other key players in the market include MedGenome Labs, CORE Diagnostics, Positive Bioscience, Neuberg Diagnostics, Leucine Rich Bio, Sarepta Therapeutics, Inc., and GSK plc.
*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*
Explore our key highlights of the report and gain a concise overview of key findings, trends, and actionable insights that will empower your strategic decisions.
| REPORT FEATURES | DETAILS |
| Base Year | 2025 |
| Historical Period | 2019-2025 |
| Forecast Period | 2026-2035 |
| Scope of the Report |
Historical and Forecast Trends, Industry Drivers and Constraints, Historical and Forecast Market Analysis by Segment:
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| Breakup by Type |
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| Breakup by Application |
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| Breakup by End User |
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| Breakup by Region |
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| Market Dynamics |
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| Supplier Landscape |
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| Companies Covered |
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