In Vitro Diagnostics (IVD) include reagents, instruments, and systems intended for use in the diagnosis of disease or other conditions, including the determination of the state of health, in order to treat or prevent disease. The reagents, instruments and systems are used in the collection, preparation, and examination of specimens taken from the human body. This includes Cardiac Disease, Hematological Disorders, Hormonal Disorders, Metabolic Disorder, Infectious Disease, IVD Analyzers, Oncology and Reproductive Health Diagnostics. Procalcitonin (PCT) Tests are carried out to diagnose and monitor sepsis, by measuring the production of PCT, a peptide precursor of the hormone calcitonin, which increases in response to a pro-inflammatory stimulus, typically as a result of bacterial infection. GlobalData uses proprietary data and analytics to provide a comprehensive report on the procalcitonin tests devices market, including market shares of different players within Belgium. Buy the latest report here.

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Data Insights Belgium Procalcitonin Tests Market Share

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In 2023, GlobalData’s Market Model methodology determined that the leading player in the procalcitonin tests market in Belgium was bioMerieux followed by F. Hoffmann-La Roche, Danaher, Abbott Laboratories, Siemens Healthineers, Bio-Rad Laboratories, Thermo Fisher Scientific, DiaSorin, Diazyme Laboratories and Quidelortho.

This includes Procalcitonin Enzyme Immunoassay Tests and Procalcitonin Other Tests which use alternative technologies, such as Fluorescence Immunoassay, latex-enhanced Immunoturbidimetric assay, and Lateral Flow immunochromatographic test strips.

The value of the procalcitonin tests devices market within Belgium was expected to be over $6m in 2023.

For the latest complete market share analysis of procalcitonin tests device market in Belgium, buy the report here.

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The medical devices pipeline data used in this article were obtained from the Medical Pipeline Products Database of GlobalData’s Medical Intelligence Center. Pipeline Products database is a comprehensive source of information on medical devices, it covers 39K products which are in development stage and intended for diagnosis, treatment, and management of diseases/conditions/symptoms directly or indirectly. The pipeline products included in the database are sourced from reliable and authenticated sources, such as company websites, SEC filings, conference presentations, analyst presentations, news releases, clinical trial registries, and grants. The information is collected by following systematic research techniques and proprietary methodology.