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Molecular Diagnostics Market size was worth USD 25 billion in 2022 and is projected to record more than 3.5% CAGR from 2023-2032. Increasing awareness regarding early disease diagnostics will accelerate industry growth.
The market for point of care molecular diagnostics is likely to surpass USD 90 billion by 2032. Growing awareness regarding early disease diagnosis and advancements in automated technologies are expected to positively influence market outlook. New-generation diagnostic solutions are offering superior levels of accuracy, convenience of use, and portability enabling early detection of an array of infectious diseases. With the rising prevalence of infectious diseases and chronic illnesses such as cancer, molecular diagnosis has emerged as a vital tool in disease management and therapy. Furthermore, the growing emphasis on precision medicine is encouraging manufacturers to design high-performance testing solutions.
Report Attribute | Details |
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Base Year: | 2022 |
Molecular Diagnostics Market Size in 2022: | USD 25 Billion |
Forecast Period: | 2023 to 2032 |
Forecast Period 2023 to 2032 CAGR: | 3.5% |
2032 Value Projection: | USD 36 Billion |
Historical Data for: | 2018 to 2022 |
No. of Pages: | 263 |
Tables, Charts & Figures: | 445 |
Segments covered: | Product, Technology, Application, End use, and Region |
Growth Drivers: |
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Pitfalls & Challenges: |
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Dearth of a streamlined regulatory framework and uniform guidelines may hamper the scope of molecular diagnostics market share. A uniform regulatory framework helps eliminate uncertainties for companies working toward the commercialization of novel drugs and therapies. However, the current challenges are causing delays in product development and market approval, forcing companies to increase their expenditure. The U.S. FDA also provides three pathways for the approval of molecular diagnostic technology based on the similarities between existing and new systems. This may limit patient access to modern and more sophisticated diagnostics technologies, negatively influencing overall industry dynamics.
Molecular diagnostics market value from PCR technology is estimated to surpass USD 22 billion by 2032. New breakthroughs in target-specific PCR systems are providing higher levels of amplification along with simultaneous detection of pathogen DNA. Additionally, PCR has an extensive range of applications in the space of healthcare and research. The technology is primarily used in the effective management of health problems such as caries, endodontic infections, oral cancer, and periodontal disease.
Molecular diagnostics market size from hospitals & clinics is anticipated to exhibit more than 3.5% CAGR between 2023 and 2032. Due to the growing disease burden, the emergence of novel epidemics & pandemics, and the increasing spending on healthcare infrastructure, the network of hospitals & clinics worldwide is set to expand significantly.
North America molecular diagnostics market size is slated to exceed USD 15 billion by 2032. North America is predicted to emerge as a hub for molecular diagnostics due to the increasing number of infectious disease outbreaks and the growing geriatric population. As per data from the Centers for Disease Control & Prevention (CDC), respiratory syncytial virus (RSV) infections lead to the hospitalization of more than 60,000-120,000 older adults in the U.S. each year with more than 6,000 deaths.
Some of the leading companies in the molecular diagnostics market include:
These firms are foraying into strategic alliances to extend collaboration and boost innovation.
The COVID-19 pandemic had a positive impact on the market with an upsurge in the demand for testing kits to detect infected patients and prevent the further spread of the virus. COVID-19 diagnostic testing solutions such as Abbott ID NOW and Cepheid GeneXpert have gained significant momentum owing to the rapid influx of government-funded R&D initiatives focusing on the development of novel solutions to counter the unprecedented crisis. In the wake of the pandemic, several regulatory agencies such as the U.S. Food & Drug Administration (FDA), and the European Commission also fostered scope for research and application of new molecular diagnostic tests.
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