The China personalized medicine market size reached USD 101.54 Million in 2025. The market is projected to reach USD 206.03 Million by 2034, growing at a CAGR of 8.18% during 2026-2034. The market is driven by robust government policy support through the 14th Five-Year Plan and strategic precision medicine initiatives, the rapid integration of artificial intelligence across drug discovery and diagnostic applications, and the expansion of digital health infrastructure including telemedicine platforms that enable personalized healthcare delivery at scale. These fundamental drivers are transforming China's healthcare landscape and expanding the China personalized medicine market share.
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Report Attribute
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Key Statistics
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| Market Size in 2025 | USD 101.54 Million |
| Market Forecast in 2034 | USD 206.03 Million |
| Market Growth Rate (2026-2034) | 8.18% |
| Key Segments | Product (Personalized Medicine Diagnostics, Personalized Medicine Therapeutics, Personalized Medical Care, Personalized Nutrition and Wellness), End Use (Hospitals, Diagnostic Centers, Research and Academic Institutes, Others), Region (North China, East China, South Central China, Southwest China, Northwest China, Northeast China) |
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Base Year
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2025
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Forecast Years
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2026-2034
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The Chinese personalized medicine market is poised for sustained expansion as the government pushes forward precision medicine programs in the 14th Five-Year Plan. Increasing access to genomic sequencing and AI-based diagnostic platforms is predicted to further personalize treatment in oncology, rare diseases, and chronic diseases. Additionally, the countrywide deployment of 5G networks and unified electronic medical records will facilitate real-time data exchange across platforms, driving exhaustive patient profiling and more precise therapeutic intervention.
AI is reshaping China's personalized medicine space at its core through the power to deliver precision diagnosis, speeding up drug discovery timelines, and enabling personalized treatment planning. AI algorithms are being used to analyze medical images, delivering diagnostic accuracy rates of more than 90 percent in some use cases such as lung nodule detection and cancer screening. In drug development, AI platforms are identifying molecular interactions and therapeutic targets with high accuracy, slashing time and cost. In addition, digital health platforms powered by AI are now combining patient information, genomics, and symptom tracking to provide personalized treatment guidelines, ensuring that more tailored medicine is available and attainable across China's varied healthcare system.
Government Policy Support Driving Strategic Precision Medicine Development
The Chinese government has established personalized medicine as a national strategic priority through comprehensive policy frameworks that provide substantial funding, regulatory support, and infrastructure development. The 14th Five-Year Plan (2021-2025) continues to emphasize interdisciplinary research and the use of artificial intelligence for biological discovery and precision medicine applications. Since the introduction of the Precision Medicine Strategy in 2015, successive Five-Year Plans have significantly advanced the application of technologies such as genetic testing and pharmacogenomics in the personalized treatment of cancer and rare diseases. China’s precision medicine market has grown rapidly in recent years and is projected to maintain strong momentum through 2030. This sustained expansion underscores its rising importance as a key growth engine within the nation’s healthcare sector, driven by increasing investment, technological innovation, and government support for advanced medical research and personalized treatment development. The government has also designated biotechnology as a strategic emerging industry, providing preferential tax treatment, subsidies, and government procurement initiatives to foster innovation. These policies are creating a favorable ecosystem for domestic and international companies to develop and commercialize personalized medicine solutions, while regulatory reforms are accelerating approval processes for innovative diagnostics and therapeutics that enable targeted patient care.
Artificial Intelligence Integration Revolutionizing Drug Discovery and Clinical Diagnostics
The China personalized medicine market is witnessing strong growth driven by the rapid integration of artificial intelligence across the healthcare value chain—from early-stage drug discovery to clinical diagnosis and treatment planning. The country’s expanding “AI + Pharma” ecosystem reflects growing investment in platforms capable of analyzing large-scale biological data and predicting individualized therapeutic strategies. A leading example is Insilico Medicine, which advanced an AI-discovered drug candidate for idiopathic pulmonary fibrosis into Phase II clinical trials, showcasing AI’s transformative potential in accelerating precision drug development. In clinical diagnostics, AI is increasingly deployed in medical imaging to enhance diagnostic accuracy and efficiency across oncology, cardiology, and respiratory care. China’s National Medical Products Administration has approved numerous AI-based diagnostic tools under its highest classification, reinforcing the country’s commitment to intelligent healthcare innovation. Rapid adoption in areas such as cancer detection, pneumonia diagnosis, and cardiac assessment highlights AI’s growing clinical relevance. Strong policy support continues to drive AI integration in pharmaceutical research, enabling faster, safer, and more cost-effective drug development. This strategic alignment between AI innovation and precision medicine is positioning China as a major global leader in next-generation healthcare technologies.
Digital Health Infrastructure Expansion Enabling Scalable Personalized Healthcare Delivery
The rapid expansion of digital health infrastructure is reshaping the delivery of personalized medicine across China’s diverse regions. Telemedicine platforms and unified electronic medical record systems are enabling more connected and data-driven healthcare ecosystems. Leading digital health providers such as Ping An Good Doctor, Alibaba Health, JD Health, and WeDoctor are leveraging AI technologies, including natural language processing and machine learning, to deliver personalized, scalable healthcare services. These platforms increasingly integrate patient records, genomic data, and treatment histories to generate precise, data-informed recommendations. The rollout of 5G networks is further advancing real-time data transmission, supporting remote consultations and continuous monitoring in areas with limited medical resources. A notable milestone in this digital transformation was the launch of Tsinghua University’s AI Agent Hospital in 2025, featuring 42 AI doctors across 21 specialties and covering hundreds of diseases. This virtual hospital exemplifies China’s commitment to using AI to address physician shortages and expand healthcare access. Aligned with the 14th Five-Year Plan for National Health Informatization, China aims to achieve full digital connectivity across public health institutions by 2025. This integrated health information infrastructure provides the foundation for implementing personalized medicine, supporting real-time clinical decision-making and holistic patient care nationwide.
Data Privacy Protection and Cross-Border Collaboration Compliance Complexity
China's evolving data protection regulatory landscape presents significant challenges for researchers and healthcare providers working with sensitive genetic and health information required for personalized medicine applications. In 2021, China adopted the Personal Information Protection Law, which provides a comprehensive legal framework for protecting personal information, including sensitive medical health data. Despite offering critical legal safeguards for processing health data, further clarification is needed regarding specific issues, including the meaning of separate consent, cross-border data transfer requirements, and exceptions for scientific research. The processing of real-world data triggers patient privacy concerns and must adhere to relevant data laws and regulations, creating possible legal impediments for researchers conducting personalized medicine studies. Challenges such as disparities in regulatory frameworks, concerns regarding data privacy, and variations in healthcare systems can obstruct the smooth integration of genomic data into clinical practice. China faces hurdles related to data accessibility, quality, and ethical concerns amid swift technological progress. The need to balance personal information protection with the public value of large-scale health data analysis remains a practical problem requiring pragmatic regulatory solutions. These compliance challenges are particularly acute for international collaborations and multi-institutional research projects that require data sharing across organizational and geographic boundaries.
Regulatory Standardization Gaps and Biomarker Validation Inconsistencies
The regulatory framework for personalized medicine diagnostics and therapeutics in China remains fragmented despite significant progress, with inconsistent standards across different testing modalities and therapeutic approaches creating barriers to widespread clinical adoption. While the National Medical Products Administration has made strides in approving innovative medical devices and diagnostics, the lack of standardized protocols for biomarker discovery, validation, and clinical implementation complicates the development and commercialization process for personalized medicine solutions. Regulatory hurdles related to the lack of standardized protocols and regulatory frameworks for biomarker-based diagnostics and therapies can impede market growth and delay the introduction of innovative products. Chinese legislators' regulatory path for medical and health information protection is more abstract and generalized compared to mature markets, with protections for the general processing of medical and health information in AI scenarios being relatively weak. The current regulatory environment requires companies to navigate multiple overlapping regulations, including the Medical Devices Supervision Regulation, Data Security Law, Personal Information Protection Law, and Administrative Regulations on Human Genetic Resources, each with different requirements and enforcement mechanisms. This regulatory complexity increases compliance costs, extends approval timelines, and creates uncertainty for companies developing personalized medicine products.
Geographic Healthcare Infrastructure Disparities Limiting Equitable Access
Significant variations exist between urban and rural healthcare infrastructure in China, with advanced personalized medicine technologies and specialized services concentrated predominantly in major metropolitan areas, including Beijing, Shanghai, and Guangdong province. Limited access to specialized genetic testing facilities, advanced diagnostic equipment, and trained personnel in rural and remote regions creates substantial inequality in precision medicine availability and quality of care. This disparity is evident in the physician-to-population ratio, as China has only a fraction of the radiologists available in developed countries, severely limiting the capacity to implement imaging-based personalized diagnostics, particularly in underserved and rural regions. Regional economic differences further exacerbate these challenges, as personalized medicine diagnostics and therapeutics often carry higher costs than traditional approaches, making them less accessible to populations in lower-income regions. While telemedicine platforms and digital health initiatives are attempting to bridge these gaps through remote consultation and diagnostic services, connectivity issues in rural areas, particularly affecting nomadic and remote communities, hamper the consistent delivery of teleconsultations and transfer of medical information. Unless these geographic disparities are systematically addressed through targeted infrastructure investments and policy interventions, large segments of China's population risk being excluded from the benefits of personalized medicine advances.
IMARC Group provides an analysis of the key trends in each segment of the China personalized medicine market, along with forecasts at the country and regional levels for 2026-2034. The market has been categorized based on product and end use.
Analysis by Product:
The report has provided a detailed breakup and analysis of the market based on the product. This includes personalized medicine diagnostics (genetic testing, direct-to-consumer diagnostics, esoteric lab services, and esoteric lab tests), personalized medicine therapeutics (pharmaceutical, genomic medicine, and medical devices), personalized medical care (telemedicine and health information technology), and personalized nutrition and wellness (retail nutrition and complementary and alternative medicine).
Analysis by End Use:
A detailed breakup and analysis of the market based on the end use have also been provided in the report. This includes hospitals, diagnostic centers, research and academic institutes, and others.
Analysis by Region:
The report has also provided a comprehensive analysis of all the major regional markets, which include North China, East China, South Central China, Southwest China, Northwest China, and Northeast China.
The China personalized medicine market is characterized by intense competition among domestic biotechnology leaders, international pharmaceutical companies, and emerging digital health platforms, each leveraging distinct competitive advantages to capture market share. Major domestic players, including BGI Genomics, Berry Genomics, and Annoroad Gene Technology, dominate the genetic testing and sequencing services segment, benefiting from government support, large-scale domestic patient populations, and cost-competitive service delivery. These companies have established strong positions through vertical integration strategies, controlling the value chain from sample collection to analysis and reporting. International pharmaceutical giants such as Roche, AstraZeneca, and Merck are focusing on developing and commercializing precision oncology therapeutics and companion diagnostics, often through strategic partnerships with Chinese companies to navigate regulatory requirements and distribution networks. Digital health platforms including Ping An Good Doctor, Alibaba Health, and JD Health are increasingly entering the personalized medicine space by integrating AI-powered diagnostic support, telemedicine services, and direct-to-consumer genetic testing offerings into their comprehensive healthcare ecosystems. Competition is also intensifying around AI-enabled clinical decision support systems, with technology companies and research institutions developing sophisticated algorithms for image analysis, treatment optimization, and predictive modeling to support personalized treatment planning.
| Report Features | Details |
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| Base Year of the Analysis | 2025 |
| Historical Period | 2020-2025 |
| Forecast Period | 2026-2034 |
| Units | Million USD |
| Scope of the Report |
Exploration of Historical Trends and Market Outlook, Industry Catalysts and Challenges, Segment-Wise Historical and Future Market Assessment:
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| Products Covered |
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| End Uses Covered | Hospitals, Diagnostic Centers, Research and Academic Institutes, Others |
| Regions Covered | North China, East China, South Central China, Southwest China, Northwest China, Northeast China |
| Customization Scope | 10% Free Customization |
| Post-Sale Analyst Support | 10-12 Weeks |
| Delivery Format | PDF and Excel through Email (We can also provide the editable version of the report in PPT/Word format on special request) |