PUBLISHER: Mordor Intelligence | PRODUCT CODE: 1851804
PUBLISHER: Mordor Intelligence | PRODUCT CODE: 1851804
The biomarkers market stood at USD 57.27 billion in 2025 and is forecast to reach USD 97.42 billion by 2030, delivering an 11.21% CAGR.

Momentum reflects artificial-intelligence-enabled discovery pipelines, wider regulatory acceptance of digital endpoints, and the push for precision medicine across oncology, immunology, neurology, and cardiology. Continued breakthrough-device designations, expanding multi-omics toolkits, and reimbursement pathways that reward targeted therapies fuel uptake of validated tests in routine care. Companion diagnostics now anchor treatment decisions, especially in oncology, where liquid biopsy and DNA methylation assays widen access to early detection and therapy matching. Investments in proteomics platforms, cloud bioinformatics, and real-world evidence solutions position vendors to capture recurring revenue from consumables, services, and software. Yet complex reimbursement policies and data-privacy regulations temper near-term adoption curves.
Chronic and life-threatening diseases are accelerating demand for refined biomarker panels. Rheumatoid arthritis registers 200,000 new U.S. cases each year, spurring adoption of 14-3-3 η protein assays that reach 74% sensitivity and 90% specificity for early detection. Age-related disorders amplify the need for minimally invasive screens; for Alzheimer's, blood-based pTau217 recently obtained FDA breakthrough designation and improves accessibility beyond cerebrospinal fluid testing . Healthcare systems pivot toward preventive medicine, prompting multiplex platforms capable of measuring markers across oncology, cardiology, and neurodegeneration in a single run. Such breadth keeps the biomarkers market on a firm growth path.
Early intervention strategies make biomarkers pivotal predictive instruments rather than confirmatory tools. CLAIRITY BREAST, an AI model that forecasts five-year breast-cancer risk from mammograms, illustrates how imaging biomarkers support proactive screening. Liquid biopsy assays detecting circulating tumor-DNA methylation now achieve 96.67% sensitivity for hepatocellular carcinoma within a 24-hour workflow . Wearables extend detection beyond clinics, with continuous monitoring of cardiometabolic indicators that trigger timely physician alerts. Artificial-intelligence-augmented analytics shorten interpretation time, easing integration into varied care settings and expanding the biomarkers market.
Divergent global rules slow commercialization. The FDA will phase out laboratory-developed-test enforcement discretion over four years, imposing device-level controls on clinical labs. Europe's In Vitro Diagnostic Regulation tightened evidence demands, while Asia-Pacific requirements remain inconsistent. Payers often require extra real-world evidence, delaying revenue for innovators and marginally cooling biomarkers market expansion.
Other drivers and restraints analyzed in the detailed report include:
For complete list of drivers and restraints, kindly check the Table Of Contents.
The cancer segment generated 46.52% of 2024 revenue within the biomarkers market. Decades of investment in genetic and protein markers, combined with fast-track companion diagnostic approvals, sustain leadership. Epigenetic liquid biopsy tests now identify multiple tumor types from a 10 ml blood draw, improving access to early treatment.
Immunological disorders are advancing at an 11.98% CAGR toward 2030, narrowing the gap. Rising autoimmune prevalence and the validation of markers such as 14-3-3 η protein in seronegative rheumatoid arthritis open new clinical workflows. Broader multiplex panels capable of tracking cytokine storms and treatment response fuel long-term growth in this slice of the biomarkers market.
Efficacy biomarkers accounted for 58.23% of 2024 spending, reflecting their use in predicting progression, guiding therapy choice, and serving as surrogate endpoints. Oncology and cardiology trials rely on established markers to cut timelines and optimize dosing.
Safety biomarkers climb fastest at 11.81% CAGR as regulators require human-relevant toxicity indicators before market authorization. AI-enabled in-vitro models read renal and hepatic stress signals within hours, supporting earlier attrition decisions. Expansion of these panels underpins risk-mitigation strategies and enlarges the biomarkers market size for pharmacovigilance.
The Biomarkers Market is Segmented by Disease (Cancer, Cardiovascular Disorders, and More), Type (Efficacy Biomarkers, Safety Biomarkers, and More), Mechanism (Genetic Biomarkers, Epigenetic Biomarkers, and More), Application (Clinical Diagnostics and More), Product (Consumables, Instruments, and More) and Geography (North America, Europe, Asia-Pacific, and More). The Market and Forecasts are Provided in Terms of Value (USD).
North America held 42.88% of global revenue in 2024 owing to FDA programs that qualify biomarkers for regulatory submissions and streamline payer coverage. Robust reimbursement and an extensive hospital network maintain high test volumes. Academic-industry consortia fast-track translation from bench to bedside, consolidating regional influence in the biomarkers market.
Asia Pacific is advancing at an 11.89% CAGR through 2030. China's 24-measure regulatory overhaul hastens innovative-device clearance, while Japan's national biotechnology plan targets 15 trillion yen market output by decade end. Aging demographics and new reimbursement codes for liquid biopsy spur rapid adoption, positioning Asia Pacific as a prime demand center for the biomarkers market.
Europe maintains consistent growth under the In Vitro Diagnostic Regulation's stringent evidence demands. Cross-border research networks produce large cohorts that validate digital and multi-omics biomarkers for chronic disease management. Middle East, Africa, and South America offer greenfield opportunities as health-system modernization and medical tourism stimulate demand for advanced diagnostics within an emerging biomarkers market ecosystem.