CAGR: 2.6% Current Market Size: USD 109.70 Billion Fastest Growing Region: APAC
Largest Market: North AmericaProjection Time: 2022-2029Base Year: 2021
Global In-vitro Diagnostics market is expected to grow from USD 109.70 billion in 2021 to USD 132.63 billion by 2029, at a CAGR of 2.6% during the forecast period 2022-2029. This market growth is mainly driven by the increasing geriatric population and the prevalence of infectious and chronic diseases.
In vitro Diagnostics (IVDs) are tests done on samples such as human blood or tissue to detect disease, infections, and conditions. These tests are usually conducted in test tubes or similar equipment. It is conducted on blood, stool, urine, and tissue samples to provide medical information used to diagnose conditions ranging from minor infections to life-threatening cancers. In addition to this, IVDs are used by patients to monitor chronic conditions such as diabetes. Hence, these tests enhance the patient's convenience through self-tests, including blood glucose monitors or pregnancy tests. Such tests can be conducted wherever the patient is, enabling them to record their condition.
The prominent IVD products include pregnancy tests, HIV tests, and COVID-19 tests, along with Cancer diagnostics, blood glucose monitoring systems, blood grouping devices, human genetic testing devices, immunoassays, and hepatitis tests. Furthermore, IVDs are also seeing significant applications in precision medicine for identifying patients who are projected to benefit from specific therapies or treatments.
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Market Dynamics:
Drivers:
Every country globally is witnessing rapid growth in both the proportion and the size of older persons in the population. For instance, according to the World Health Organization (WHO), 1 in 6 people around the globe will be aged more than 60 years by 2030. This growth in the geriatric population creates increased demand for healthcare services. Moreover, the incidence of chronic diseases such as diabetes, heart disease, and cancer among the aging population is comparatively higher than in the younger population. For instance, as per the World Health Organization (WHO), the prevalence of chronic diseases was expected to rise by 57% by December 2020. In addition, emerging markets such as China and India were expected to be hardest hit by chronic diseases due to population growth. These diseases include chronic respiratory diseases, cancer, cardiovascular diseases, and diabetes. The prevalence of such diseases has fuelled demand for in vitro diagnostics.
Precision medicine is mainly aimed at targeting accurate treatments to the right patients at the right time. In vitro diagnostics are used in this sector to identify patients who are expected to benefit from specific therapies or treatments. Hence, an overall growth of the precision medicine sector drives the In Vitro Diagnostics market growth.
Restraints:
Due to related high costs, there is a major shortage of diagnostics solutions and equipment in low- and middle-income countries (LMICs). This has been the major restraint in the global in the vitro diagnostics market. In addition, sophisticated and expensive medical equipment is seeing comparatively less adoption in rural and semi-rural areas across the LMIC settings. For instance, according to the Centers for Medicare & Medicaid Services, the U.S. federal agency, healthcare costs will skyrocket to $4.3 trillion in 2021. This increase in healthcare costs is anticipated to hamper the growth of the market to some extent during the forecast period.
Opportunities:
A companion diagnostic device provides information that is crucial for effective and safe usage of a corresponding therapeutic product. These devices are usually developed in collaboration with drug development companies to help doctors in excluding or select particular patients for treatment. Moreover, recently, the U.S. Food and Drug Administration (FDA) issued draft guidance that outlined considerations for the labeling and development of in vitro companion diagnostics to support indicated usage for several drug or biologic oncology products. Such regulations associated with in vitro companion diagnostics have further created lucrative growth opportunities for the market.
Challenges
The European regulations for medical devices (EU MDR) and In-vitro Diagnostic Devices (EU IVDR) have replaced In-vitro Diagnostic Directive (IVDD), old legislation, in May 2022. These regulations require manufacturers in IVD market to make considerable changes in data reporting, product development, and quality assurance. This is expected to pose challenges such as higher costs and longer timelines for new product development in front of in vitro diagnostics device manufacturers.
Segmentation Analysis:
The global In-vitro Diagnostics market has been segmented based on product and service, technology, application, end-user, and regions.
By Product and Service
The product and service segment includes reagents & kits, instruments, services, and data management software. The reagents & kits segment led the In-vitro Diagnostics market with a market share of around 64.10% in 2021. This is attributed to the upsurge in demand for COVID-19 test kits & reagents for the detecting proteins from the COVID-19 virus in respiratory or in serum or blood samples. In addition, rising product development trend in the market creates lucrative growth opportunities for the market. For instance, In June 2022, Agilent Technologies Inc., American analytical instrumentation development and manufacturing company, launched the In Vitro Diagnostic Regulation (IVDR) (EU) 2017/746 compliant Class A products, including kits, instruments, and reagents.
By Technology
The technology segment includes immunoassay/ immunochemistry, clinical chemistry, molecular diagnostics, hematology, microbiology, coagulation and hemostasis, urinalysis, and other technologies. The molecular diagnostics segment led the In-vitro Diagnostics market with a market share of around 35.1% in 2021. The growth of this segment is mainly driven by continuous technological evolution and the introduction of new technology. For instance, in February 2020, FIND, an international non-profit organization, introduced an expression of interest (EOI) for test developers of in vitro diagnostics (IVDs) for detection of SARS-CoV-2 nucleic acid (molecular tests).
By End User
The end users segment includes hospital laboratories, clinical laboratories, point-of-care testing centers, academic institutes, patients, and other end users. The hospital laboratories segment led the In-vitro Diagnostics market with a market share of around 36.10% in 2021. The ongoing development trend of automated IVD systems for hospitals and laboratories to provide accurate, efficient, and error-free diagnoses has driven the growth of this segment. Furthermore, in March 2022, Applied BioCode, an IVD manufacturer, signed an agreement with Hardy Diagnostics, a manufacturer of microbiology products in the U.S., for the distribution of the MDx-3000 System for the diagnosis of gastrointestinal infections and upper respiratory infections. This system is expected to be used by high-complexity laboratories. Such developments are expected to create lucrative growth opportunities for the growth of this segment.
By Regional Analysis:
The regions analyzed for the In-vitro Diagnostics market include North America, Europe, South America, Asia Pacific, and the Middle East, and Africa. The North American region dominated the In-vitro Diagnostics market and held the 38.02% share of the market revenue in 2021.
Global In-vitro Diagnostics Market- Country Analysis:
In Europe, Germany is one of the largest market shareholders in the In-Vitro Diagnostic Market In addition, this country has a strong healthcare system, especially in regard to hospital beds, infrastructure, equipment, and trained staff.
Germany's In-vitro Diagnostics market size was valued at USD 10.97 billion in 2021 and is expected to reach USD 13.22 billion by 2029, at a CAGR of 2.5% from 2022 to 2029.
A number of factors, including the growing number of private hospitals, rising demand for personalized medicine & point-of-care testing, and an upsurge in the number of independent testing laboratories, have driven the growth of Germany In-vitro Diagnostics market. Moreover, according to the International Diabetes Federation, an umbrella organization of over 230 national diabetes associations, the prevalence rate of diabetes in adults across Germany was 15.3% in 2020. This has further created the demand for In-vitro Diagnostics in the country.
China's In-vitro Diagnostics market size was valued at USD 21.94 billion in 2021 and is expected to reach USD 26.22 billion by 2029, at a CAGR of 2.4% from 2022 to 2029. China has become a prominent In-vitro Diagnostics markets due to economic growth, the aging population, and expanding basic health insurance sector. In addition, by 2030, the Chinese government has planned a broader healthcare ecosystem of about 16 trillion RMB with continuous optimization of healthcare management & services.
Furthermore, according to the National Health Commission of the People's Republic of China, about 1.71 million cases of infectious diseases were reported in December 2019 in the country. This prevalence of infectious diseases has boosted demand for In-vitro Diagnostics in the country.
India's In-vitro Diagnostics market size was valued at USD 4.39 billion in 2021 and is expected to reach USD 5.38 billion by 2029, at a CAGR of 2.8% from 2022 to 2029. India is one of the strongest growing economies in Asia. This country is seeing increased government spending on the development of healthcare facilities. For instance, in December 2019, the ministry of health and family welfare of the Indian government introduced its plans to partner with private firms operating in diagnostic services to provide enhanced diagnostic services under the Ayushman Bharat-Pradhan Mantri Jan Arogya Yojana (AB-PMJAY).
Key Industry Players Analysis:
To increase their market position in the global In-vitro Diagnostics business, top companies are focusing on tactics such as adopting new technology, mergers & acquisitions, product developments, collaborations, and partnerships, joint ventures, etc.
Latest Development:
Report Metrics
Report Attribute |
Details |
Study Period |
2021-2029 |
Base year |
2021 |
CAGR (%) |
2.6% |
Market Size |
109.70 billion in 2021 |
Projection period |
2022-2029 |
Projection unit |
Value (USD) |
Segments covered |
Product and service, technology, application, end user, and Regions |
Report Scope |
Revenue Projection, competitive landscape, company ranking, growth factors, and trends |
Companies covered |
Roche Diagnostics, Siemens Healthineers, Danaher Corporation, Abbott, Thermo Fisher Scientific, Johnson & Johnson, Becton, Dickinson and Company, Bio-Rad Laboratories, Sysmex Corporation, among others |
By Product and Service |
|
By Technology |
|
By Application |
|
By End User |
|
Regional scope |
|
Scope of the Report
Global In-vitro Diagnostics Market by Product and Service:
Global In-vitro Diagnostics Market by Technology:
Global In-vitro Diagnostics Market by Application:
Global In-vitro Diagnostics Market by End User:
Global In-vitro Diagnostics Market by Region:
Global In-Vitro Diagnostic Market size is USD 109.70 billion in 2021
Global In vitro Diagnostics market will command to USD 132.63 billion by 2029, at a CAGR of 2.6% from 2022 to 2029
North American region dominated the In-vitro Diagnostics market and held the 38.02% share of the market revenue in 2021
Leading market players active in the global In vitro Diagnostics market are Roche Diagnostics, Siemens Healthineers, Danaher Corporation, Abbott, Thermo Fisher Scientific, Johnson & Johnson, Becton, Dickinson and Company, Bio-Rad Laboratories, and Sysmex Corporation among others.
Increasing geriatric population and prevalence of infectious and chronic diseases is primarily driving the growth of the In vitro Diagnostics market.
In March 2022, Roche Diagnostics, a Swiss multinational healthcare company, collaborated with Bristol Myers Squibb, an American multinational pharmaceutical company, to support the advancements in personalized healthcare with the help of digital pathology solutions.
Political Factors- The European regulations for medical devices (EU MDR) and In-vitro Diagnostic Devices (EU IVDR) have replaced In-vitro Diagnostic Directive (IVDD), old legislation, in May 2022. These regulations require manufacturers in IVD market to make considerable changes in data reporting, product development, and quality assurance. This is expected to pose challenges such as higher costs and longer timelines for new product development in front of in vitro diagnostics device manufacturers. For instance, in December 2019, the ministry of health and family welfare of the Indian government introduced its plans to partner with private firms operating in diagnostic services to provide enhanced diagnostic services under the Ayushman Bharat-Pradhan Mantri Jan Arogya Yojana (AB-PMJAY).
Economical Factors- Due to related high costs, there is a major shortage of diagnostics solutions and equipment in low- and middle-income countries (LMICs). This has been the major restraint in the global in the vitro diagnostics market. In addition, sophisticated and expensive medical equipment is seeing comparatively less adoption in rural and semi-rural areas across the LMIC settings. For instance, according to the Centers for Medicare & Medicaid Services, the U.S. federal agency, healthcare costs will skyrocket to $4.3 trillion in 2021. This increase in healthcare costs is anticipated to hamper the growth of the market to some extent during the Projection period.
Social Factor- China has become a prominent In-vitro Diagnostics markets due to economic growth, the aging population, and expanding basic health insurance sector. In addition, by 2030, the Chinese government has planned a broader healthcare ecosystem of about 16 trillion RMB with continuous optimization of healthcare management & services. Furthermore, according to the National Health Commission of the People's Republic of China, about 1.71 million cases of infectious diseases were reported in December 2019 in the country. This prevalence of infectious diseases has boosted demand for In-vitro Diagnostics in the country.
Technological Factors- The rising product development trend in the market creates lucrative growth opportunities for the market. For instance, In June 2022, Agilent Technologies Inc., American analytical instrumentation development and manufacturing company, launched the In Vitro Diagnostic Regulation (IVDR) (EU) 2017/746 compliant Class A products, including kits, instruments, and reagents. FIND, an international non-profit organization, introduced an expression of interest (EOI) for test developers of in vitro diagnostics (IVDs) for detection of SARS-CoV-2 nucleic acid (molecular tests).
Environmental Factors- According to various studies, the rising pollution increases the the occurence of chronic diseases. The increasing pollution causes multiple diseases ranging from minor infections to life-threatening cancers. In addition to this, IVDs are used by patients to monitor chronic conditions such as diabetes. Every country globally is witnessing rapid growth in both the proportion and the size of older persons in the population. For instance, according to the World Health Organization (WHO), 1 in 6 people around the globe will be aged more than 60 years by 2030. This growth in the geriatric population creates increased demand for healthcare services.
Legal Factors- Roche Diagnostics, a Swiss multinational healthcare company, collaborated with Bristol Myers Squibb, an American multinational pharmaceutical company, to support the advancements in personalized healthcare with the help of digital pathology solutions. Siemens Healthineers AG, a German medical device company, partnered with United Nations Children's Fund UNICEF to optimize Point-of-Care diagnostics networks. The partnership is aimed at strengthening the fragile health systems across sub-Saharan Africa.
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