Various different tests and diagnostic tools that are done outside of the body are part of in vitro diagnostics. The market for these is changing because of new technologies, more people knowing about healthcare, and a greater need for personalized treatment.
A lot of point-of-care tests (POCT) are being done in in vitro diagnostics. Because they are done close to the patient, these tests give quick results that are very important in situations because they help doctors make quick choices and cut down on diagnosis time.
DNA, RNA, and protein analysis are the focus of molecular diagnostics, which has advanced significantly. Diagnostic systems are using more PCR and NGS approaches. Through integration, sickness diagnosis and treatment design may be more accurate and complete.
Liquid biopsy, a growing cancer screening method, may identify blood biomarkers. This non-invasive technique is transforming cancer surveillance by enabling early identification, therapy response evaluation, and real-time genetic mutation tracking.
Using antibodies to measure analytes, immunoassays are being developed. Diagnostic tests are becoming more accurate as assays get more sensitive and specific. Multiplex immunoassays may detect several analytes concurrently, improving diagnostic profiles.
In vitro diagnostics and digital health are a major trend. Remote patient monitoring, wearable devices, and smartphone apps simplify chronic illness monitoring and treatment. These technologies enable diagnostic data collection and interpretation.
The integration of molecular diagnostics into point-of-care settings is a major development. Portable molecular testing technologies are enabling quick diagnosis at the patient's bedside or in community healthcare settings, especially in resource-poor places.
The COVID-19 pandemic has increased worldwide emphasis on infectious illnesses, which has led to further research and development of diagnostics. fast antigen, nucleic acid amplification, and serological assays are vital in infectious disease diagnostics' fast evolution.
Companion diagnostics is rising due to personalised medicine, which tailors therapies to each patient. Therefore, these tests help identify patients who will benefit from specific medications, which improves treatment results and reduces bad effects.
The IVD sector is affected by changing regulations and worldwide harmonization initiatives. Using rules and quality control to improve diagnostic test uniformity and reliability. This protects patients and simplifies market entry for firms.
Telemedicine is attracting more individuals to home diagnostics. Patients are taking charge of their health via self-administered testing, remote monitoring gadgets, and telehealth platforms. This causes diagnostic service decentralization.
Emerging markets affect IVD more than mature markets. Diagnostic testing is becoming more accessible worldwide due to greater healthcare expertise, infrastructural improvements, and growing disposable budgets in poorer nations. This trend creates new market growth potential.
The In Vitro Diagnostics (IVD) Market Size was valued at USD 94.12 Billion in 2023 and is projected to grow from USD 96.19 Billion in 2024 to USD 112.02 Billion by 2032, exhibiting a compound annual growth rate (CAGR) of 1.92% during the forecast period (2024 - 2032). Increased instances of chronic diseases and rising health concerns are the key market drivers enhancing the market growth.
Source Secondary Research, Primary Research, MRFR Database and Analyst Review
Roche and Hitachi High-Tech have renewed their ten-year contract to collaborate on the development and production of diagnostic solutions in May 2024. By the end of the year, the companies intend to introduce new analytical units, including the cobas c 703 and cobas ISE neo, as well as a completely automated mass spectrometry integration solution, the cobas Mass Spec solution. GlobalData's analysis indicated that the In Vitro Diagnostics (IVD) market was valued at approximately $49.6 billion last year. The in vitro diagnostic analyzer sub-section of the market was valued at approximately $4.8 billion last year and is anticipated to generate sales exceeding $7.8 billion by 2033..
In recent months, Roche has received numerous approvals from the US Food and Drug Administration (FDA) for its molecular assays, which are conducted on cobas systems. In March, the company obtained US approval for the first-ever blood screening test for malaria. Healthcare professionals can screen for the disease in blood, organ, and tissue donors by administering the test on the polymerase chain reaction (PCR)-based cobas 6800/8800 systems.
NeoDx Biotech Labs, a Bengaluru-based startup, has introduced a Real-time PCR-Technology-based in vitro diagnostic (IVD) kit for Ankylosing Spondylitis in September 2023. This kit enables healthcare services to enhance their testing capabilities.. The HLA-B27 RT-PCR detection kit for Exon 2/Exon 3 is a real-time PCR test instrument that is employed to identify Human Leukocyte Antigen B27 in whole blood. HLA-B27 is significantly associated with the inflammatory disorders Ankylosing Spondylitis (AS), Psoriasis, Inflammatory Bowel Disease, and Reactive Arthritis.
HLA-B27 testing can be advantageous for the early identification and treatment of these illnesses. These diseases are estimated to affect approximately 0.25% of the Indian population. In a recent study published in the Indian Journal of Rheumatology, various factors associated with Axial Spondyloarthritis were examined. The results indicated that nearly 70% of AS patients are misdiagnosed for the first three years or more, which exacerbates their condition. The assay has been subjected to a comprehensive performance assessment and testing, and it has been shown to be highly sensitive and specific, as well as compatible with the majority of commercially available RT-PCR systems. The kit is equipped with all the necessary reagents and controls to conduct the experiments.
January 2024: Qiagen received FDA clearance for its NeuMoDx CT/NG Assay 2.0, which enhances testing for Chlamydia trachomatis and Neisseria gonorrhoeae.
February 2024: Siemens Healthineers and Hermes Pardini Group are creating an automated lab using the Atellica Solution, aiming to improve operational efficiency and test accuracy.
In Vitro Diagnostics (IVD) market is being driven by the rising chronic diseases and technological upgrades. The high prevalence of chronic and infectious diseases, the rising use of point-of-care (POC) diagnostics, cutting-edge technologies in in-vitro diagnostic products, and growing acceptance of companion diagnostics and personalised medicine are all factors contributing to the growth of the IVD market. The Centres for Disease Control and Prevention (CDC) estimate that 18.2 million persons in the United States aged 20 and older have coronary artery disease (CAD) in 2021. In the United States, heart disease is the main factor in fatalities. The market is driven by the rising prevalence of chronic diseases, which raises the demand for expensive diagnostic treatments.
The utilisation of cutting-edge technology in the IVD industry is another factor contributing to the expansion of the current market. Traditional diagnostics have given way to a new generation of gene-level diagnostics, representing a paradigm change. This was made feasible by integrating cutting-edge technologies into the IVD platform, including genetic testing, molecular diagnostics, polymerase chain reaction (PCR), and next-generation sequencing (NGS). Additionally, more product launches with cutting-edge features are anticipated to fuel the industry. For instance, Agilient Technologies introduced IVD-compliant tools, kits, and reagents in June 2022 for usage in accordance with the new IVDR legislation of the European Union.
Furthermore, since there is a rising need for IVD kits and reagents for the rapid and precise diagnosis of SARS-CoV2 virus infection across the population, the COVID-19 pandemic brought in vitro diagnostics (IVD) market to the fore. Due to the fact that include analysing diverse biological samples, the COVID-19 epidemic had a favourable effect on the market. This aided in the diagnosis of contagious illnesses like COVID-19. An important element in containing the COVID-19 outbreak was testing. The article "The Impact of COVID-19 on the Invitro Diagnostic Industry," which appeared in April 2021, underlined the importance of IVD testing using human body samples to fight COVID-19. Due to the increased usage of pandemic-required advancements like remote collections and digital pathology, the sector experienced tremendous growth after COVID-19. Thus, driving the revenue.
The in vitro diagnostics (IVD) market based on product & service includes Reagents & Kits, Instruments, and Data management Software. The reagents & kits segment dominated the market. Due to considerable R&D initiatives being performed by key market players for the development of novel reagents, the category is anticipated to maintain its leadership while increasing at the quickest CAGR over the forecast period. Companies can now concentrate on lucrative niche markets in the IVD industry thanks to the introduction of kits that enable speedier cancer detection. LiquidPlex Dx and FusionPlex Dx cancer diagnostic kits, for instance, were introduced by Invitae in February 2022 to enable effective management of cancer patients with medication and prompt delivery of the necessary information.
The market segmentation of based on application, includes Infectious Diseases, and Non-Infectious Diseases. The category for infectious diseases has the largest market share. The identification of infectious disease-causing bacteria is made possible by IVDs. HIV/AIDS, TB, hepatitis, and pneumonia are the most frequently occurring life-threatening illnesses. In addition, major market participants are collaborating to make it easier for patients and healthcare professionals to obtain high-quality, cutting-edge laboratory services.
Figure 1 In Vitro Diagnostics (IVD) Market, by Application, 2022 & 2032 (USD Billion)
Source Secondary Research, Primary Research, MRFR Database and Analyst Review
By region, the study provides the market insights into North America, Europe, Asia-Pacific and Rest of the World. The North American In Vitro Diagnostics (IVD) market area will dominate this market, owing to an increase in the instances of chronic diseases and rising geriatric population.
Further, the major countries studied in the market report are The US, Canada, German, France, the UK, Italy, Spain, China, Japan, India, Australia, South Korea, and Brazil.
Figure 2 In Vitro Diagnostics (IVD) MARKET SHARE BY REGION 2022 (USD Billion)
Source Secondary Research, Primary Research, MRFR Database and Analyst Review
Europe market accounts for the second-largest market share due to the technological advancements and rise in demands for point-of-care testing. Further, the German market held the largest market share, and the UK market was the fastest growing market in the European region
The Asia-Pacific In Vitro Diagnostics (IVD) Market is expected to grow at the fastest CAGR from 2023 to 2032. This is due to rising incomes and governmental support within the region. Moreover, China’s In Vitro Diagnostics (IVD) market held the largest market share, and the market of In Vitro Diagnostics was the fastest growing market in the Asia-Pacific region.
Leading market players are involving themselves in various research and development related activities to strengthen their product lines, which will help the market grow more. Market players are also adopting a number of strategic activities to expand their footprint, with important market developments including new product launches, contract & agreements, mergers & acquisitions, increased investments, and partnerships with other organizations. To grow and sustain in a competitive and rising market climate, industry must offer cost-effective items.
Manufacturing locally to minimize operational costs is one of the key business tactics used by manufacturers in the industry to benefit clients and increase the market sector. In recent years, the industry has offered some of the most significant advantages to medicine. Major players in the market of including Abbott Laboratories, Bio-Rad Laboratories Inc., Hoffman-LA Roche AG, Grifols S.A., bioMerieux S.A., DiaSorin S.p.A., Ortho Clinical Diagnostics, Qiagen N.V., Siemens AG, Becton Dickinson & Company, and others, are attempting to increase market demand by investing in research and development operations.
A wide variety of healthcare goods are discovered, developed, produced, and sold by Abbott Laboratories (Abbott), including branded generic medications, diagnostic tools and procedures, and infant, child, and adult nutritional supplements. The business also sells a range of medical devices, such as those for neuromodulation, electrophysiology, rhythm control, vascular and structural cardiac devices, and heart failure. The business also sells dietary supplements, minerals, and nutrition goods.
It runs manufacturing sites all around the world and has research and development centres in the US, China, Colombia, India, Singapore, Spain, and the UK. In October 2020, The healthcare business Abbott Laboratories (NYSE ABT), and Quanterix Corporation, a company that digitises biomarker analyses to improve the science of precision health, have agreed into a non-exclusive royalty-bearing licence agreement. Abbott now has non-exclusive access to Quanterix's patents pertaining to bead-based technology for use in in vitro diagnostic (IVD) applications.
Grifols SA is a pharmaceutical and chemical manufacturing firm called. The company is dedicated to improving the health and wellbeing of individuals all over the world. Research, development, production, and commercialization of plasma-derived medicines, hospital pharmacy products, and clinically applicable diagnostic technology are its main areas of concentration. The business creates plasma-derived protein treatments for people with rare, persistent, and fatal infections.
For use in biotechnology research, producing pharmaceutical and diagnostic goods, and clinical trials, Grifols provides biological materials. For blood banks, clinical laboratories, and transfusion centres, Grifols offers solutions for hemostasis, immunoassay, and transfusion medicine. In December 2021, The TÜV SÜD Product Service and BSI, both of which are EU-designated notified bodies under the new regulation, have granted Grifols its first Technical Documentation Assessment and Quality Management System certificates under the Medical Devices Regulation (IVDR). Grifols is a leader in the development of plasma-derived therapies and cutting-edge diagnostic solutions.
January 2021 The quick handheld TBI blood test developed by Abbott was given FDA approval. The pioneering test is used to evaluate patients with minor traumatic brain injuries (TBIs) and concussions. In addition, Abbott introduced the RealTime SARS-CoV-2 assay, a PCR-based test, in March 2020 for the diagnosis of COVID-19, and BioMedomics introduced a point-of-care COVID-19 test in May 2020 that can identify antibodies in blood within 15 minutes.
January 2022 In order to enhance patient care, Roche Diagnostics (Switzerland) introduced the Cobas pulse system, a blood glucose management tool with mobile digital health capabilities.
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