Global Isothermal Nucleic Acid Amplification Technology (INAAT) Market- Key Developments
Global Isothermal Nucleic Acid Amplification Technology (INAAT) Market- Key Trends
Increasing Product Launches
Increasing product launch of loop-mediated isothermal amplification for the isothermal nucleic acid amplification technology is expected to drive the global isothermal nucleic acid amplification technology market growth over the forecast period. For instance, in May 2022, Meridian Bioscience is a life science company that develops, manufactures, markets, and distributes a broad range of innovative diagnostic and life science products., launched two new innovative isothermal amplification products named Lyo-Ready Direct DNA LAMP Saliva Mix and Lyo-Ready Direct RNA/DNA LAMP saliva mix. These are used for direct detection of DNA and RNA in point of care dagnostics assays.
Global Isothermal Nucleic Acid Amplification Technology (INAAT) Market – Impact of Coronavirus (COVID-19) Pandemic
Since the COVID-19 virus outbreak in December 2019, the disease has spread to over 100 countries across the globe, and the World Health Organization declared it a public health emergency on January 30, 2020.
COVID-19 affected the economy in three main ways: by directly affecting the production and demand of drugs, by creating disruptions in distribution channels, and through its financial impact on firms and financial markets. Due to nationwide lockdowns, several countries such as China, India, Saudi Arabia, the U.A.E., Egypt, and others faced problems regarding transportation of drugs from one place to another.
However, the COVID-19 pandemic had a positive impact on the global isothermal nucleic acid amplification technology (INAAT) market growth, owing to increasing usage of and product approvals and launches of isothermal nucleic acid amplification technology during the pandemic. For instance, in March 2020, Abbott company provides from newborns to aging adults, from nutrition and diagnostics through medical care and pharmaceutical therapy. , received the U.S. Food and Drug Administration approval for the emergency use of ID NOW COVID-19, an instrument-based, isothermal, rapid system for the qualitative finding of disease.
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