Global In-Vitro Diagnostics Market

In-Vitro Diagnostics Market Size, Share, Growth Analysis, By Product & Service(Reagents & Kits, Instruments), By Technology(Clinical chemistry, Molecular diagnostics), By Application(Infectious diseases, Diabetes), By End-User(Standalone laboratories, Hospitals) - Industry Forecast 2024-2031


Report ID: SQSG35G2015 | Region: Global | Published Date: February, 2024
Pages: 157 | Tables: 124 | Figures: 77

In-Vitro Diagnostics Market Insights

Global In-Vitro Diagnostics (IVD) Market size was valued at USD 117.8 billion in 2019 and is poised to grow from USD 121.69 billion in 2023 to USD 157.78 billion by 2031, growing at a CAGR of 3.3% during the forecast period (2024-2031).

The growing opportunities in unexploited emerging markets with enhanced health infrastructure, rising unfulfilled medical needs, increasing prevalence of chronic diseases, and more demand for cutting-edge testing methodologies have been predicted to serve as the driving force behind the proliferation of the in vitro diagnostics market. The emergence of personalized medicine as an individualized treatment approach tailored to patient’s specific genetic, molecular, and clinical contexts is also a contributing factor that is shaping the IVD market. On the spectrum of IVDs, companion diagnostics, a unique subset, take an active part in assessing patients appropriate for therapies or those at risk of adverse drug reactions or toxicity. These individualized interventions not only increase the treatment efficacy but also contain the healthcare costs by avoiding wasteful treatments, thus emphasizing market expansion.

IVD industry operates in a regulated environment to confirm patient safety and accuracy of the test. Getting regulatory approvals for an innovative IVD test may be time-consuming and be resource intensive. The rigorous regulatory standards, imposed by the regulatory institutions like the FDA and similar bodies worldwide, might slow down the rapid entrance of new tests and technologies, which in turn may become an obstacle in the growth path of the IVD market. It is forecasted that the market will face growth due to the arrival of products that have improved versatility. For instance, in June 2022, Agilent Technologies introduced IVD-compliant instruments, kits, and reagents that follow the new European Union IVDR regulation and further and greater the demand for and usage of IVD devices. This growth is also supported by increased investment from leading industrial actors aimed at research and development projects to develop new products and explore new applications of IVD technologies. For instance, in February 2022 Thermo Fisher Scientific Inc. introduced the Renvo Rapid PCR Test, which is aimed at airborne viruses, including SARS-CoV-2 pathogens. The test is performed on samples collected using the Aerosol Sense Sampler. Therefore, their immediate coming onto the market can be expected not only to encourage the rise of the IVD market but also to become its major drivers.

US In-Vitro Diagnostics Market is poised to grow at a sustainable CAGR for the next forecast year.

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In-Vitro Diagnostics (IVD) Market size was valued at USD 117.8 billion in 2019 and is poised to grow from USD 121.69 billion in 2023 to USD 157.78 billion by 2031, growing at a CAGR of 3.3% during the forecast period (2024-2031).

The In-Vitro Diagnostics market is relatively fragmented, with a high level of competition. Companies are working on new product launches and other initiatives to provide better equipment to their customers and expand their companies globally. These industry leaders are expanding their client base in a variety of ways, and many organizations are forming strategic and creative partnerships with other start-up businesses in order to increase market share and profitability. 'Roche Diagnostics', 'Siemens Healthineers', 'Abbott Laboratories', 'Danaher Corporation', 'Thermo Fisher Scientific', 'Sysmex Corporation', 'bioMerieux SA', 'Becton, Dickinson and Company', 'Ortho-Clinical Diagnostics', 'QIAGEN N.V.', 'Beckman Coulter, Inc.', 'Hologic, Inc.', 'Bio-Rad Laboratories', 'Agilent Technologies', 'Illumina, Inc.', 'Cepheid', 'PerkinElmer, Inc.', 'Bruker Corporation', 'Luminex Corporation', 'DiaSorin S.p.A.'

The centralized laboratory using automated analytical testing techniques to identify target analytes continues to be the predominant laboratory testing paradigm in use today. This pattern is already well-established in the fields of clinical chemistry and hematology, and it is currently spreading to others like immunoassays and molecular diagnostics.

The market's reagent segment contains elements, solutions, or preparations that are chemical, biological, or immunological and that the maker intends to utilize throughout the in vitro diagnosis procedure. Manufacturers frequently lease equipment rather than selling it outright to customers since many diagnostic platforms are expensive. In these agreements, the leasing is linked to agreements for the long-term purchase of related reagents or tests for the equipment.

The in-vitro diagnostics market size in North America was the largest in 2020, and it's expected to hold this position during the forecast period. This is ascribed to the region's well-integrated healthcare system, patients' increased knowledge of healthcare issues, patients' adoption of cutting-edge therapies, and an increase in healthcare spending overall. However, the Asia-Pacific region is expected to see significant growth due to rising healthcare costs, a sizable patient population with chronic illnesses that necessitate IVD testing, and rising disposable incomes. In addition, the Asia-Pacific in-vitro diagnostics market is anticipated to rise rapidly in India and China.

In-Vitro Diagnostics (IVD) Market size was valued at USD 117.8 billion in 2019 and is poised to grow from USD 121.69 billion in 2023 to USD 157.78 billion by 2031, growing at a CAGR of 3.3% during the forecast period (2024-2031).

The in vitro diagnostics (IVD) market presents a dynamic competitive landscape characterized by a diverse array of players ranging from established multinational corporations to innovative startups. The companies continuously engage in research and development activities to introduce innovative diagnostic solutions, expand their market reach, and strengthen their competitive position. However, the market also sees vigorous competition from niche players specializing in specific diagnostic segments or cutting-edge technologies, fostering innovation and driving market growth. 'Roche Diagnostics', 'Siemens Healthineers', 'Abbott Laboratories', 'Danaher Corporation', 'Thermo Fisher Scientific', 'Sysmex Corporation', 'bioMerieux SA', 'Becton, Dickinson and Company', 'Ortho-Clinical Diagnostics', 'QIAGEN N.V.', 'Beckman Coulter, Inc.', 'Hologic, Inc.', 'Bio-Rad Laboratories', 'Agilent Technologies', 'Illumina, Inc.', 'Cepheid', 'PerkinElmer, Inc.', 'Bruker Corporation', 'Luminex Corporation', 'DiaSorin S.p.A.'

The growing pressure of chronic diseases, majorly discussed by organizations is a major issue that is being seen as a challenge to all the healthcare systems. Non-Communicable Diseases (NCDs) including cardiovascular diseases, cancer, chronic respiratory diseases and diabetes are responsible for a significant proportion of the morbidity and mortality. In-Vitro Diagnostics (IVD) contribute to the early diagnosis of such diseases while allowing healthcare professionals to immediately provide an adequate treatment. Through the prompt determination of disease, IVD technologies enables early treatment that in turn ensures positive patient outcomes as well as helps to lower the overall pressure on the healthcare system. However, in its September 2022 brochure the World Health Organization emphasizes the overwhelming burden of NCDs. These conditions are responsible for a very high number of deaths worldwide. Coronary heart disease and other cardiovascular diseases, however, become the first reason for death among all diseases, in front of cancer cases, chronic respiratory ones and diabetes. Data evidence the need for effective strategies that can collectively address these diseases.

Shift towards Sustainable and Resilient Infrastructure: The increase in the burden of diseases has urged medical device companies to speed up the design of highly advanced diagnostic devices. In addition, hospitals and laboratories are mainly relying on point-of-care devices due to their capability to provide immediate and real-time data. Point-of-Care (PoC) testing is a diagnostic method which is performed close to the patient, with minimal blood volume needed, and which offers rapid test results crucial for clinical decision making, making the physician to initiate timely treatment without waiting for the central laboratory results. Therefore, the demand for these instruments will increase, which will lead to an increase in the need for the in vitro diagnostics devices. Moreover, an increase in the launch of new and advanced products are set to drive the industry development. For example, In January 2023, FUJIFILM Sonosite, Inc. came up with the new Sonosite PX ultrasound system in India to replace the traditional system. The aim is to enhance clinician ergonomics and streamline efficiency.

In 2022, North America contributed to the major share of the in vitro diagnostics market, and it is considered to maintain its top position during the market forecast period. Therefore, the main reason for their dominance is that many of the leading players are involved. Apart from this, the region also has witnessed technological upgrades in manufacturing sector for in vitro diagnostics which is another driving factor for this market.

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Global In-Vitro Diagnostics Market

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