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A Closer Look into FDA-EUA Approved Diagnostic Techniques of Covid-19

ACS Infect Dis. 2021-09; 
Hyunju Oh, Hyunjeong Ahn, Anubhav Tripathi
Products/Services Used Details Operation
Proteins, Expression, Isolation and Analysis … However, these assays can only be performed at high-containment laboratories, limiting the accessibility of the assays, and, currently, cPass SARS-CoV-2 Neutralization Antibody Detection Kit by GenScript USA Inc. is the only serological device utilizing this assay technique.() … Get A Quote

摘要

The 2019 coronavirus disease (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 virus, caused a worldwide pandemic in 2020 and is the most urgent health issue worldwide. In this review, we highlight the details of Food and Drug Administration-Emergency Use Authorizations approved diagnostics kits, focusing on the similarities and differences. It is essential to understand the currently available options and the advantages and disadvantages each provides to select the appropriate products that maximize the testing efficiency. We believe this work will provide a holistic evaluation of the current COVID-19 diagnostic resources, including variations across the countries, and guide developing ... More

關鍵詞

COVID-19, FDA-EUA, molecular diagnostics, multicountry analysis, serological diagnostics
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