In January 2022, SANSURE BIOTECH INC., an in-vitro diagnostic developments supplier, declared that its HPV DNA Diagnostic Kit (HPV 13+2)’ was authorized by the China National Medical Products Administration (NMPA).Food and Drug Administration (FDA) approval for its product, the BD onclarity HPV Assay to be utilized with the ThinPrep Pap Test. In February 2023, BD and Company (Becton, Dickinson, and Company), an American multinational medical technology corporation, received U.S.In August of 2022, Microsoft and SRL Diagnostics created an instrument based on artificial intelligence to aid in quicker cervical cancer diagnosis. In the future, the expanding use of artificial intelligence in product development will positively affect the global cervical cancer diagnostics market. Artificial Intelligence (AI) Impact Analysis Due to the urgent need for crisis equipment in Ukraine, the EU has deployed services from its medical rescue reserves, including generators, medical equipment, temporary shelter units, and technical tools for threats to public health, such as biological, chemical, radiological, and nuclear hazards. Thus, the EU has mobilized all possible aid to assist the Ukrainian crisis service. Millions of individuals lack access to basic necessities. Continued hostilities endanger the lives of civilians and cause severe damage to housing, water and electrical reserves, heating, and public institutions such as schools and hospitals. Since the conflict in Ukraine has evolved into a full-blown humanitarian catastrophe. The Russia-Ukraine conflict has significantly impacted the global market for cervical cancer diagnostics. This includes developing point-of-care testing devices, self-sampling kits, and telemedicine-based screening solutions.įor more details on this report Request for Sample: Opportunities exist for businesses to develop and market innovative diagnostic solutions that can improve screening accuracy, accessibility, and convenience. There is a growing emphasis on cervical cancer prevention through awareness campaigns and screening programs. In one study, the lifetime probability of a false positive for annual, 3-year, and 5-year triage testing (either LBC with HPV reflex or vice versa) was 35.1%, 13.4%, and 8.2%, respectively. Increasing false positive results are impeding the growth of the global market for cervical cancer diagnostics over the forecast period. Market Restraintsįalse-positive tests are screening tests that return a positive result but are not subsequently validated with high-grade cervical intraepithelial neoplasia (CIN). The increasing number of product approvals for cervical cancer diagnostics by distinct regulatory bodies is driving the global cervical cancer diagnostics market growth during the forecast period. In the United States in 2023, the American Cancer Society estimates that there will be over 13,960 new cases of invasive cervical cancer and approximately 4,310 deaths due to cervical cancer. The rising incidence of cervical cancer worldwide is propelling the growth of the cervical cancer diagnostics market over the forecast period. Hoffmann-La Roche Ltd., Guided Therapeutics, Olympus, Cardinal Health, Siemens Healthcare, Hologic, Inc., Quest Diagnostics, QIAGEN, OncoHealth Corp., Arbor Vita, Zilico Ltd., and among others. The major global players in the market include Abbott Laboratories, Becton, Dickinson and Company, F. North America is anticipated to hold approximately 38.9% of the global cervical cancer diagnostics market due to the region’s increasing market developments and expanding awareness. The global cervical cancer diagnostics market is segmented based on test type, age group, distribution channel, and region. The market for cervical cancer diagnosis is expected to grow due to rising awareness and increasing prevalence in emerging economies. Cervical cancer affects the cells in the cervix and can be diagnosed through tests such as a Pap smear, colposcopy, and ECC.
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