Press release
Global Antinuclear Antibody (ANA) Test Market Size, Growth Analysis Report, Forecast to 2027
The global ANA test market is anticipated to grow significantly at a CAGR of 12.3% during the forecast period (2021-2027). The ANA test market is segmented based on the product type, test type, disease type, and end-users. Among the test type, the market is segmented into indirect immunofluorescence, enzyme-linked immunosorbent assay (ELISA), and multiplex testing. Besides, the key companies across the globe are adopting different business strategies including expanding their geographic presence, R&D activities, new product approvals, mergers & acquisitions, partnerships, and collaborations to increase market share.(Get 15% Discount on Buying this Report)
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Further, in February 2019, Grifols, a producer of plasma-derived medicines and one of the leaders in the development of innovative diagnostic solutions, has announced that the US Food and Drug Administration (FDA) approved the Procleix Babesia assay, a qualitative assay for the detection of the ribosomal RNA from 4 Babesia species (B. microti, B. duncani, B. divergens, B. venatorum) in samples of individual or around 16 pooled lysed specimens from human donors, including donors of whole blood and blood components for transfusion. The assay is utilizing Nucleic Acid Testing (NAT) for blood screening.
A Full Report of Global Antinuclear Antibody (ANA) Test Market is Available at: https://www.omrglobal.com/industry-reports/antinuclear-antibody-ana-test-market
In Addition, in June 2018, Grifols' latest diagnostic examinations for Antineutrophil Cytoplasmic Antibodies (ANCA)-associated vasculitis and lupus were approved by the US FDA. These tests enabled labs to use immunofluorescence assays to standardize and speed up diagnosis. The FDA's recent approvals would enable laboratories to diagnose autoimmune diseases like lupus, scleroderma, and vasculitis more accurately and efficiently. Apart from it, in October 2020, ZEUS Scientific has announced the received approval from the US Food and Drug Administration (FDA) for Emergency Use Authorization (EUA) for its in vitro ELISA diagnostic test for the qualitative detection of IgG antibodies to the SARS-CoV-2 virus in human serum and plasma. This test is readily available in all clinical laboratories since it is in stock. However, the various approvals by the US FDA for the assays, diagnostics test, and others of the key players are to propel the growth of the global ANA test market.
Global ANA Test Market Report Segment
By Product Type
Assay Kits & Reagents
Antinuclear Antibody Test System
Antinuclear Antibody Test Software
By Test Type
Indirect Immunofluorescence
Enzyme-Linked Immunosorbent Assay (ELISA)
Multiplex Testing
By Disease Type
Systemic Lupus Erythematosus
Sjögren’s Syndrome
Rheumatoid Arthritis
Scleroderma
Others (Addison Disease And Pulmonary Fibrosis)
By End-User
Hospitals
Clinical Laboratories
Global ANA Test Market Report Segment by Region
North America
United States
Canada
Europe
UK
Germany
Italy
Spain
France
Rest of Europe
Asia-Pacific
China
India
Japan
South Korea
Rest of Asia-Pacific
Rest of the World
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