The point
of care molecular diagnostics market is experiencing steady
growth, with a CAGR of ~6% driven by increasing demand for rapid and
decentralized diagnostic solutions. Key factors propelling market
expansion include the rising prevalence of infectious diseases, growing
adoption in resource-limited settings, and advancements in miniaturized
diagnostic technologies. However, challenges such as regulatory complexities
and high initial costs for POC molecular platforms may hinder widespread
adoption.
Point of care molecular diagnostics refers to advanced
diagnostic testing conducted at or near the patient site, enabling rapid
detection of pathogens and genetic markers. Unlike traditional lab-based
molecular diagnostics, POC molecular testing integrates sample preparation,
amplification, and detection into a compact system, reducing turnaround time
from hours to minutes. These diagnostics leverage technologies like PCR and
isothermal amplification, ensuring high sensitivity and specificity in detecting
infectious diseases, genetic conditions, and oncology markers. Their
significance lies in improving early diagnosis, guiding timely treatment, and
enhancing healthcare accessibility, particularly in remote or under-resourced
areas.
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Widespread infectious disease burden accelerating market
growth
The increasing prevalence of infectious diseases is a
primary factor fueling the expansion of the POC Molecular Diagnostics market.
The growing global burden of respiratory infections, sexually transmitted
diseases, and emerging viral outbreaks necessitates rapid and decentralized
diagnostic solutions. Conventional laboratory-based molecular diagnostics,
while highly accurate, often require centralized facilities and lengthy
turnaround times, delaying treatment decisions. POC molecular platforms bridge this
gap by delivering near-instant results at the patient’s location, facilitating
prompt clinical intervention. Additionally, healthcare systems in low- and
middle-income countries benefit from these rapid diagnostics, as they reduce
the dependency on specialized infrastructure and skilled personnel. The
COVID-19 pandemic further underscored the importance of fast, accurate
molecular testing at the point of care, accelerating investment in portable
diagnostic devices. As healthcare providers prioritize early disease detection
and containment strategies, the demand for POC molecular diagnostics continues
to surge, reshaping infectious disease management worldwide.
Microfluidics revolutionizing POC molecular testing
Microfluidic-based POC molecular diagnostics represent a
significant innovation enhancing the market’s effectiveness and adoption.
Microfluidics enables the miniaturization and automation of molecular assays,
integrating multiple testing steps—sample extraction, amplification, and
detection—into a single, compact chip. These systems require minimal sample
volumes, reducing reagent costs while maintaining high analytical sensitivity.
Additionally, microfluidic platforms improve assay reproducibility and reliability,
addressing variability concerns in traditional manual methods. The portability
of microfluidic-based devices makes them ideal for field settings, rural
clinics, and emergency response situations, where timely diagnostics are
critical. Moreover, advancements in lab-on-a-chip technology have streamlined
complex workflows, enabling non-specialists to conduct sophisticated molecular
testing with minimal training. As the technology matures, microfluidic POC
diagnostics are expected to drive broader adoption, particularly in infectious
disease surveillance, antimicrobial resistance monitoring, and personalized
medicine applications.
Competitive Landscape Analysis
The global point of care molecular diagnostics market is
marked by the presence of established and emerging market players such as Abbott;
F. Hoffmann-La Roche AG; QIAGEN; Danaher; Bio-Rad Laboratories,
Inc.; bioMérieux; Agilent Technologies, Inc.; Nova Biomedical; Nipro
Diagnostics and Thermo Fisher Scientific among others. Some of the
key strategies adopted by market players include new product development,
strategic partnerships and collaborations, and geographic expansion.
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Market Segmentation
This report by Medi-Tech Insights provides the size of
the point of care molecular diagnostics market at the regional- and
country-level from 2023 to 2030. The report further segments the market based
on technology, application and end-user.
- Market
Size & Forecast (2023-2030), By Technology, USD Million
- PCR-based
- Genetic
Sequencing-based
- Microarray-based
- Others
- Market
Size & Forecast (2023-2030), By Application, USD Million
- Infectious
Diseases
- Cancer
- Endocrinology
- Hematology
- Others
- Market
Size & Forecast (2023-2030), By End-user, USD Million
- Hospitals
- Diagnostic
Laboratories
- Home
Care Settings
- Others
- Market
Size & Forecast (2023-2030), By Region, USD Million
- North
America
- US
- Canada
- Europe
- UK
- Germany
- France
- Italy
- Spain
- Rest
of Europe
- Asia
Pacific
- China
- India
- Japan
- Rest
of Asia Pacific
- Latin
America
- Middle
East & Africa
Medi-Tech Insights
is a healthcare-focused business research & insights firm. Our clients
include Fortune 500 companies, blue-chip investors & hyper-growth
start-ups. We have completed 100+ projects in Digital Health, Healthcare IT,
Medical Technology, Medical Devices & Pharma Services in the areas of
market assessments, due diligence, competitive intelligence, market sizing and
forecasting, pricing analysis & go-to-market strategy. Our methodology
includes rigorous secondary research combined with deep-dive interviews with
industry-leading CXO, VPs, and key demand/supply side decision-makers.
Contact:
Ruta Halde
Associate, Medi-Tech Insights
+32 498 86 80 79
info@meditechinsights.com
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