According to the current analysis of Reports and Data, the global In-Vitro Diagnostics (IVD) Quality Control Market was valued at USD 881.8 Million in 2018 and is expected to reach USD 1229.3 Million by year 2026, at a CAGR of 4.3%. —
IVD quality controls are tests used to authenticate the consistency of IVD testing system to confirm precision of test findings and assess the influence of factors such as environmental conditions and operator’s performance on test results. Key recent developments: in June 2019, Illumina, Inc. announced the launch of VeriSeq NIPT Solution v2, a CE-IVD; next-generation sequencing (NGS)-based approach to noninvasive prenatal testing (NIPT), delivers the most comprehensive view of the fetal genome compared to other CE-IVD NIPT products.
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Key players mentioned in the research report are:
Agilent Technologies, Abbott Diagnostics, Becton, Dickinson and Company, BioMerieux, Inc., Bio-Techne, Bio-Rad Laboratories, Inc., DiaSorin, Fortress Diagnostics, Future Diagnostics Solutions, Helena Laboratories, Hologic, Inc., Illumina, Laboratory Corporation, Quidel Corporation, Roche Diagnostics, Randox Laboratories Ltd., Seracare Life Sciences, Inc., Sun Diagnostics, LLC., Sero AS, Sysmex Corporation, Surmodics, Inc., Siemens Healthcare GmbH, Technopath Clinical Diagnostics, and Thermo Fisher Scientific, Inc.
In terms of applications, the global In-Vitro Diagnostics (IVD) Quality Control market can be segmented into:
In terms of types, the global In-Vitro Diagnostics (IVD) Quality Control market can be segmented into:
Data Management Solutions
Quality Assurance Services
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For geographical segmentation, regional supply, application-wise, and type-wise demand, key players, and others, this report covers the following regions: North America, Europe, Asia-Pacific, South America, and Middle East & Africa. The report sheds light on the competitive landscape of the market that covers the product offerings, services, market shares, and business overview. This In-Vitro Diagnostics (IVD) Quality Control Market research report covers various dynamic aspects like the market drivers, restraints and challenges, and growth prospects. The prominent and leading companies are profiled in the report.
Further key findings from the report suggest:
• The American Clinical Laboratory Association (ACLA) states that more than 7.5 billion lab tests are performed in U.S. annually and 80% of clinical decisions are taken after lab testing
• In December 2018, BioMérieux announced its culture bottles BACT/ALERT® BPA and BPN have received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for quality control testing of leukocyte-reduced apheresis platelet (LRAP) units with the BACT/ALERT® VIRTUO® fully automated blood culture system
• In-Vitro Diagnostics (IVD) Quality Control Market is fastest growing at a CAGR of 3% in Asia Pacific owing to rising incidence of IVD tests in developing countries such as India and China due to upsurge in number of clinical laboratories, global awareness among patients
• FDA is encouraging convergence of regulatory systems for medical devices, which is anticipated to boost trade, while protecting public health through regulatory means
• Data Management Solutions segment is accounted to be the second-leading segment which is valued at USD 155.6 million because it gives access to LIS and easy for managing test results of patients and even popular due to dependable laboratory outcomes
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