Canada In-Vitro Diagnostics Market - Growth, Trends, COVID-19 Impact, and Forecasts (2022 - 2027)

Canada In-Vitro Diagnostics Market - Growth, Trends, COVID-19 Impact, and Forecasts (2022 - 2027)

The Canada in-vitro diagnostics market is expected to register a CAGR of 5.2% over the forecast period, 2022-2027.

The emergence of the SARS-CoV-2 virus has increased lab testing demands to keep pace with suspected cases of COVID-19. Thus, the recent outbreak of COVID-19 has had a positive impact on the in-vitro diagnostics industry, as it involves the testing of various biological samples. Likewise, the growing need for early diagnosis of COVID-19 patients provided lucrative opportunities for the key players to expand their geographical reach within the country and has led to new product launches and approvals. For instance, in February 2021, Thermo Fisher Scientific received Health Canada authorization for its Applied Biosystems TaqPath COVID-19 HT Kit, to give a significant boost to laboratories' COVID-19 testing capabilities. Thus, such developments are likely to bolster the growth of the in-vitro diagnostics market in the country.

Moreover, the factors that are responsible for the growth of this market include the increasing use of point-of-care (POC) diagnostics; advanced technologies; and increasing awareness and acceptance of personalized medicine and companion diagnostics.

In-vitro diagnostics products and consumables are extremely valuable for disease prevention, detection, and management. The demand for point-of-care diagnostics is increasing owing to the high burden of various diseases in this country. According to the data published by GLOBOCAN 2020, it was estimated that in 2020, approximately 274,364 Canadians were diagnosed with cancer. Likewise, as per the 2022 report from the Public Health Agency of Canada (PHAC), there were 604 cases of monkeypox as of July 20, 2022. Therefore, the rising cases of these infectious diseases will help boost the demand for in-vitro diagnostics to aid in the diagnosis or detection of these diseases, in turn driving the market growth.

In addition, the emerging technological innovations in healthcare, such as biosensors, lab-on-a-chip, wearable devices, and point of care (POC) diagnostics, are increasingly becoming an important part of the healthcare landscape. POC diagnostics are no longer limited to simple tests and can now be used for diagnosing serious conditions. Market players in this region are focusing on market development strategies such as product development, merger and acquisition, and partnerships. For instance, in March 2021, QIAGEN N.V. launched the QIAcube Connect MDx, a flexible platform for automated sample processing for molecular diagnostic laboratories in Canada. Also, in April 2020, Seegene, Inc. received the Health Canada (HC) authorized interim order which allows the import and sale in Canada of Seegene's Allplex 2019-nCoV Assay, a Real-time RT-PCR test for SARS-CoV-2, the novel coronavirus responsible for the COVID-19 disease.

Thus, owing to all these market development strategies, coupled with the growing burden of several diseases in the country, the market for in-vitro diagnostics is expected to grow in Canada. However, stringent regulations and cumbersome reimbursement procedures are likely to hinder the market's growth.

Key Market TrendsReagent Segment is Expected to hold the Significant Market Share Over the Forecast Period

The reagent segment of the market studied includes chemical, biological, or immunological components, solutions, or preparations intended by the manufacturer to be used during the in-vitro diagnosis process. Reagents are an integral part of the in-vitro diagnostics testing procedure. They are used for a wide variety of disease diagnoses. With the increasing complexity of diseases and demand for early diagnosis, there is an increased use of complex reagent combinations in laboratories to diagnose these diseases from biological samples. In addition, for the assessment of a patient’s general health by a physician, the major information comes from the information supplied by the diagnostics laboratory, where the importance of diagnostic reagents becomes evident. Many diagnostic companies have an excess of more than 50% of sales from consumables, such as assays and reagents, and such agreements guarantee the generation of cyclic revenues associated with the sale of reagents and other consumables.

Furthermore, increasing competition, pressures laboratories to continuously improve quality and provide rapid results, this demand drives the need for reagents that perform multiple functions efficiently. For instance, in May 2021, LaunchWorks, a contract development and manufacturing organization (CDMO) in molecular diagnostics, and Canadienzyme, a Canadian biotech spin-off company, entered into a collaboration to produce a new RT-qPCR Master Mix, an RT-qPCR testing reagent.

Thus, these factors are likely to drive the demand for the reagents segment throughout the forecast period.

Competitive Landscape

The Canadian In-Vitro Diagnostics market is moderately competitive and consists of several major players. In terms of market share, a few of the major players currently dominate the market. In addition, the rising need for diagnostics due to the rising prevalence of diseases and the advances in IVD is helping a few other smaller players enter the market. Some of the major players in the market are Becton Dickinson and Company, BioMerieux, Bio-Rad Laboratories Inc., Danaher Corporation, and Thermo Fisher Scientific, among others.

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1 INTRODUCTION
1.1 Study Assumption and Market Definition
1.2 Scope of the Study
2 RESEARCH METHODOLOGY
3 EXECUTIVE SUMMARY
4 MARKET DYNAMICS
4.1 Market Overview
4.2 Market Drivers
4.2.1 Increasing Use of Point-of-Care (POC) Diagnostics and Advancements in Technology
4.2.2 Increasing Awareness and Acceptance of Personalized Medicine and Companion Diagnostics
4.3 Market Restraints
4.3.1 Stringent Regulations and Cumbersome Reimbursement Procedures
4.4 Porter's Five Force Analysis
4.4.1 Threat of New Entrants
4.4.2 Bargaining Power of Buyers/Consumers
4.4.3 Bargaining Power of Suppliers
4.4.4 Threat of Substitute Products
4.4.5 Intensity of Competitive Rivalry
5 MARKET SEGMENTATION (Market Size by Value - USD million)
5.1 By Test Type
5.1.1 Clinical Chemistry
5.1.2 Molecular Diagnostics
5.1.3 Hematology
5.1.4 Immuno Diagnostics
5.1.5 Other Tests
5.2 By Product
5.2.1 Instrument
5.2.2 Reagent
5.2.3 Other Products
5.3 By Usability
5.3.1 Disposable IVD Devices
5.3.2 Reusable IVD Devices
5.4 By Application
5.4.1 Infectious Disease
5.4.2 Diabetes
5.4.3 Cancer/Oncology
5.4.4 Cardiology
5.4.5 Autoimmune Disease
5.4.6 Nephrology
5.4.7 Other Applications
5.5 By End Users
5.5.1 Diagnostic Laboratories
5.5.2 Hospitals and Clinics
5.5.3 Other End Users
6 COMPETITIVE LANDSCAPE
6.1 Company Profiles
6.1.1 Siemens AG
6.1.2 Danaher Corporation
6.1.3 F. Hoffmann-La Roche AG
6.1.4 Becton, Dickinson and Company
6.1.5 Bio-Rad Laboratories Inc.
6.1.6 Abbott Laboratories
6.1.7 Arkray Inc.
6.1.8 Hologic, Inc
6.1.9 Thermo Fischer Scientific Inc.
6.1.10 Qiagen N.V.
7 MARKET OPPORTUNITIES AND FUTURE TRENDS

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