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. Epidermal Growth Factor Receptor gene (EGFR) Tests are carried out to detect mutations within this receptor gene in Non-Small Cell Lung Cancer (NSCLC) tumor cells; the outcome of which may determine if EGFR-targeted tyrosine kinase inhibitors such as gefitinib and erlotinib may be beneficial for treating NSCLC. GlobalData uses proprietary data and analytics to provide a comprehensive report on the egfr tests devices market, including market shares of different players within Australia. Buy the latest report here.
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In 2023, GlobalData’s Market Model methodology determined that the leading player in the egfr tests market in Australia was Thermo Fisher Scientific followed by Qiagen, F. Hoffmann-La Roche, Abbott Laboratories and Agilent Technologies.
The EGFR Tests includes EGFR Immunohistochemistry Tests, EGFR Nucleic Acid Amplification Tests (NAATs), EGFR Sanger Sequencing Tests, and EGFR Other Tests which include In Situ Hybridisation (ISH) and Mass Array.
The value of the egfr tests devices market within Australia was expected to be over $0.3m in 2023.
For the latest complete market share analysis of egfr tests device market in Australia, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
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.
