COVID-19 Diagnostics Market to Surpass Revenues of USD 13 Billion in 2020
|
By LabMedica International staff writers Posted on 10 Dec 2020 |

Illustration
The global COVID-19 diagnostics market is expected to reach revenues of over USD 13 billion in 2020 and is projected to grow at a CAGR of around (9)% during the period 2020-2026, driven by the surging demand for rapid testing across the globe. However, once COVID-19 vaccines are released in the market, the novel coronavirus will no longer be given pandemic status and COVID-19 will become like any other normal infectious disease, thus reducing the demand for test kits in the market.
These are the latest findings of Arizton Advisory and Intelligence (Chicago, IL, USA), a provider of market intelligence reports and advisory and consulting services.
Countries across the globe are conducting mass testing for COVID-19 to diagnose and isolate affected patients, helping to contain the spread of the coronavirus. As the number of people with the disease increases and other existing diagnostic techniques such as polymerase chain reaction (PCR) take longer, the demand for rapid testing is surging. People feel that they can be severely affected by the disease by the time they provide a sample for the test and receive the results. Rapid testing can provide results within 24 hours or less. As the number of samples increases, labs are using more rapid testing to increase the number of tests performed. Rapid tests are also being used as a priority in hospitals as the waiting period for the test results has increased to more than a week in some places.
Based on product, the need to perform rapid testing for the detection of coronavirus is driving the demand for consumables, including biomarkers and reagents, including substrates, enzymes, electrolytes, specific proteins, lipids, and point-of-care test kits, as they obtain quick and accurate results for diagnosing diseases, including COVID-19. On the basis of type of test, the reverse transcription-polymerase chain reaction (RT-PCR) segment holds a share of over 75% of the global COVID diagnostics market as RT-PCR testing is considered exceptionally reliable. The COVID-19 diagnostics market is witnessing increasing uptake of PCR testing for reliable and quick diagnosis. The WHO has recommended it as a gold standard test for COVID-19 diagnosis, leading to higher usage of PCR testing among countries across the world. The demand for PCR-based tests has increased by 300 times, as compared to the pre-COVID-19 situation.
Based on technology, the molecular segment holds the largest share of the global COVID-19 diagnostics market, as most of the immunoassays had demonstrated limited sensitivity and specificity during the initial days of the pandemic. Immunoassay tests had also produced several false positive and false negative results, forcing healthcare providers to look for alternative testing methods. This has resulted in greater preference for the use of molecular techniques such as PCR for accurate diagnosis. However, vendors have now come up with high sensitivity and specificity immunoassay tests that deliver superior results. By end-user, the diagnostic laboratories segment dominates the global COVID-19 diagnostics market with the highest share, as the majority of public and private labs are focusing on the diagnosis of COVID-19 samples during the pandemic.
Geographically, APAC accounted for the largest share of the global COVID-19 diagnostics market at around 42% in 2019. This was primarily due to the larger population and large numbers of tests conducted by countries such as China, India, and Singapore in the region. China, Japan, India, South Korea, and Australia are the major revenue contributors to the APAC COVID-19 diagnostics market. APAC is expected to remain the largest market for COVID-19 diagnostics during the forecast period as its higher population will increase the target pool of people requiring diagnosis and improvement in the region’s healthcare infrastructure. In addition, the rising purchasing power for healthcare services and growing focus on early diagnosis and prevention programs such as mass testing in the region are encouraging more people to get diagnosed for COVID-19.
Related Links:
Arizton Advisory and Intelligence
These are the latest findings of Arizton Advisory and Intelligence (Chicago, IL, USA), a provider of market intelligence reports and advisory and consulting services.
Countries across the globe are conducting mass testing for COVID-19 to diagnose and isolate affected patients, helping to contain the spread of the coronavirus. As the number of people with the disease increases and other existing diagnostic techniques such as polymerase chain reaction (PCR) take longer, the demand for rapid testing is surging. People feel that they can be severely affected by the disease by the time they provide a sample for the test and receive the results. Rapid testing can provide results within 24 hours or less. As the number of samples increases, labs are using more rapid testing to increase the number of tests performed. Rapid tests are also being used as a priority in hospitals as the waiting period for the test results has increased to more than a week in some places.
Based on product, the need to perform rapid testing for the detection of coronavirus is driving the demand for consumables, including biomarkers and reagents, including substrates, enzymes, electrolytes, specific proteins, lipids, and point-of-care test kits, as they obtain quick and accurate results for diagnosing diseases, including COVID-19. On the basis of type of test, the reverse transcription-polymerase chain reaction (RT-PCR) segment holds a share of over 75% of the global COVID diagnostics market as RT-PCR testing is considered exceptionally reliable. The COVID-19 diagnostics market is witnessing increasing uptake of PCR testing for reliable and quick diagnosis. The WHO has recommended it as a gold standard test for COVID-19 diagnosis, leading to higher usage of PCR testing among countries across the world. The demand for PCR-based tests has increased by 300 times, as compared to the pre-COVID-19 situation.
Based on technology, the molecular segment holds the largest share of the global COVID-19 diagnostics market, as most of the immunoassays had demonstrated limited sensitivity and specificity during the initial days of the pandemic. Immunoassay tests had also produced several false positive and false negative results, forcing healthcare providers to look for alternative testing methods. This has resulted in greater preference for the use of molecular techniques such as PCR for accurate diagnosis. However, vendors have now come up with high sensitivity and specificity immunoassay tests that deliver superior results. By end-user, the diagnostic laboratories segment dominates the global COVID-19 diagnostics market with the highest share, as the majority of public and private labs are focusing on the diagnosis of COVID-19 samples during the pandemic.
Geographically, APAC accounted for the largest share of the global COVID-19 diagnostics market at around 42% in 2019. This was primarily due to the larger population and large numbers of tests conducted by countries such as China, India, and Singapore in the region. China, Japan, India, South Korea, and Australia are the major revenue contributors to the APAC COVID-19 diagnostics market. APAC is expected to remain the largest market for COVID-19 diagnostics during the forecast period as its higher population will increase the target pool of people requiring diagnosis and improvement in the region’s healthcare infrastructure. In addition, the rising purchasing power for healthcare services and growing focus on early diagnosis and prevention programs such as mass testing in the region are encouraging more people to get diagnosed for COVID-19.
Related Links:
Arizton Advisory and Intelligence
Latest Industry News
- Natera’s Signatera Earns IVDR Certification for Solid Tumor MRD Testing
- Eurobio Scientific Completes Acquisition of CareDx Lab Products Division
- Blood-Based CRISPR Test for Tuberculosis Gains Regulatory Approval in Colombia
- Merck KGaA to Acquire Bio-Techne, Expanding Life Science Portfolio
- Agilent Strengthens Pathology Capabilities Through Biocare Acquisition
- Partnership Integrates Automated DNA Extraction with Single-Molecule Digital PCR
- Project Aims to Develop First Single-Cell Assay for ADC Therapies
- Agreement Supports pTau217-Based Alzheimer’s Blood Test Development
- Collaboration Aims to Broaden Access to NETosis-Linked Disease Testing
- Partnership Aims to Improve Transplant Monitoring Across Care Continuum
- QIAGEN Enhances QIAcuity Platform with Gene Expression and Multiplexing Tools
- Partnership Expands Ultrasensitive Blood-Based Diagnostics for Hematologic Malignancies
- Genetic Testing Program Expands Detection of Alpha-1 Antitrypsin Deficiency
- Collaboration Advances ctDNA-Guided Development in Metastatic Colorectal Cancer
- Open-Source Consortium Aims to Standardize Digital Pathology Workflows
- Diazyme Laboratories Acquires Carolina Liquid Chemistries
Channels
Clinical Chemistry
view channel
Blood Test Improves Alzheimer’s Diagnosis and Management Across Care Settings
Early and accurate identification of Alzheimer’s disease remains challenging in routine care, particularly outside memory clinics. Confirmation often depends on positron emission tomography (PET) imaging... Read more
New Immunoassay Enables Ultrasensitive Blood-Based Tau Tangle Measurement
Alamar Biosciences (Fremont, CA, USA) has introduced the first commercial immunoassay for enhanced microtubule binding region tau (eMTBR-Tau). The assay is available within the NULISAseq Neuro 220 multiplexed... Read moreMolecular Diagnostics
view channel
Blood Test Achieves Improved Detection of Advanced Precancerous Colorectal Lesions
Colorectal cancer is the second-leading cause of cancer-related death in the United States, yet screening uptake remains suboptimal. More than 50 million eligible adults are not up to date with recommended... Read more
Community-Based Genetic Screening Reaches Rural and Vulnerable Populations
Many adults inherit genetic changes that increase their risk for cancer and cardiovascular disease, yet access to testing often remains concentrated in large medical centers. Reaching rural and socially... Read moreHematology
view channel
New Biomarkers Predict Resistance to Targeted Therapy in Rare Blood Cancer
Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare and aggressive leukemia with limited treatment options and a poor prognosis. Although tagraxofusp is the first approved targeted therapy for... Read more
AI Decision Support System Guides Treatment Selection for Complex Blood Cancers
Treatment selection for hematologic malignancies often requires clinicians to synthesize clinical histories, genomic alterations, prior therapies, and rapidly evolving drug options. These complex decisions... Read moreImmunology
view channel
Diagnostic Models Detect Hidden Eye Abnormalities After Mild COVID-19
Persistent ocular symptoms after COVID-19 can severely affect reading, work, and daily tasks, yet standard eye exams often reveal no clear abnormalities. Patients experiencing photophobia, eye pain, and... Read more
Anti-Lipid Antibody Biomarkers May Identify Early Lyme Disease and Persistent Symptoms
Lyme disease is often missed during its earliest and most treatable stage, while current serologic assays cannot distinguish active infection from prior exposure. Nearly half a million Americans are diagnosed... Read more
Emergency Department Opt-Out Testing Program Identifies Undiagnosed HIV
Undiagnosed HIV continues to drive avoidable morbidity and transmission, with many people identified only after substantial immune damage has occurred. In England, about one in 20 people living with HIV... Read more
Immune Biomarkers Could Identify Risk of Chronic Critical Illness on ICU Admission
Severe traumatic injury can trigger immune and organ dysfunction that complicates recovery in the intensive care unit. A subset of patients develop chronic critical illness, defined as dependence on intensive... Read moreMicrobiology
view channel
Bacterial Growth Assay Predicts COVID-19 Severity From Plasma
COVID-19 presents with a wide clinical spectrum, from mild illness to severe, life-threatening disease. Early differentiation between patients likely to remain mild and those at risk of severe progression... Read more
Gut Microbiome Analysis Identifies Frailty-Related Signatures in Older Adults
Frailty in older adults is marked by increased vulnerability to disease, falls, functional decline, and death, yet its biological drivers remain incompletely understood. Because the gut microbiota influences... Read morePathology
view channel
FDA-Approved Companion Diagnostic Detects PTEN Loss in Prostate Cancer
Prostate cancer is the most common cancer among U.S. men, with more than 300,000 new cases and over 36,000 deaths each year. As targeted therapies emerge for biomarker-defined subgroups, laboratories need... Read more
New AI Test Delivers Rapid Breast Cancer Recurrence Predictions
Recurrent breast cancer remains a persistent driver of morbidity and retreatment, and current risk stratification often depends on genomic assays that are costly and slow. Waiting weeks for results can... Read moreTechnology
view channel
Training Device Improves Accuracy of Pooled Molecular Diagnostics
High-throughput molecular diagnostics have transformed infectious disease detection, but many workflows remain difficult to execute accurately without extensive training. Sample pooling can cut per‑test... Read more
New CE-Certified Software Advances Whole-Genome Cancer Testing
European hospitals are increasingly using comprehensive tumor genomics to guide therapy, but routine whole genome sequencing (WGS) requires validated, regulation-compliant workflows. A newly CE-certified... Read more
National Rare Disease Registry Standardizes Genetic and Clinical Data for Coordinated Care
Rare diseases collectively impose a significant clinical burden despite their individual rarity, often involving multisystem presentations and prolonged diagnostic journeys. Limited specialist expertise... Read moreIndustry
view channel
Natera’s Signatera Earns IVDR Certification for Solid Tumor MRD Testing
Natera’s Signatera has received certification as a Class C device under the European Union’s In Vitro Diagnostic Regulation (IVDR), becoming the first personalized MRD test for solid tumors to achieve... Read more
Eurobio Scientific Completes Acquisition of CareDx Lab Products Division
Eurobio Scientific has closed the acquisition of CareDx AB in Sweden and its fully owned subsidiaries in the United States and Australia that constitute CareDx’s Lab Products division. The business will... Read more
Blood-Based CRISPR Test for Tuberculosis Gains Regulatory Approval in Colombia
Colombia remains a high-priority setting for tuberculosis, with a growing need for diagnostics that complement existing testing strategies and improve access to earlier diagnosis. Solutions that function... Read more








