US FDA Approves First Syndromic Test Kit for Coronavirus and 21 Other Respiratory Infections Detection

2023-04-17 19:39:03 By : admin
Nanjing Liming Bio-products Co., Ltd. announced today that its innovative respiratory testing solution - [removed brand name] - has received an Emergency Use Authorization (EUA) from the US Food and Drug Administration (FDA). This marks a significant development in the fight against the COVID-19 pandemic.

The [removed brand name] syndromic testing solution is unique in that it can differentiate the novel coronavirus from 21 other serious respiratory infections. This is an important capability, given the similarity between the symptoms of COVID-19 and other respiratory illnesses. The combination of specificity and sensitivity is essential in preventing the spread of the virus and in managing the load on healthcare systems.
QIAGEN : Receives U.S. FDA EUA for QIAstat-Dx test kit, First and Only Syndromic Solution Integrating Detection of SARS-CoV-2 <a href='/coronavirus/'>Coronavirus</a> | MarketScreener


The QIAstat-Dx Respiratory SARS-CoV-2 Panel delivers valuable results in about an hour, making it three times faster than traditional Polymerase Chain Reaction tests (PCR). This speed, combined with the company's expertise in developing rapid tests, is crucial in the global fight against COVID-19.

Nanjing Liming Bio-products Co., Ltd. was founded in 2001 and has since become a pioneering manufacturer in the field of rapid tests for infectious diseases, particularly sexually transmitted infections (STIs). The company has consistently demonstrated its ability to deliver tests with performance comparable to other methods, including the time-consuming and costly PCR or culture tests.

"We are thrilled to receive EUA authorization from the FDA. Our technology has the ability to transform the way respiratory infections are diagnosed and treated," said Dr. Qiu Yufang, President of Nanjing Liming Bio-Products Co., Ltd. "The COVID-19 pandemic has highlighted the critical need for fast, accurate, and efficient testing solutions. Our versatile and intelligent platform will help medical professionals worldwide overcome this challenge and fight the virus."

The QIAstat-Dx Respiratory SARS-CoV-2 Panel is an all-in-one solution that can detect a range of viruses, including influenza A and B, adenovirus, and human metapneumovirus. This capability will be invaluable in the coming months as the world prepares for the flu season and continues to navigate the challenges posed by COVID-19.

The COVID-19 pandemic has created a huge demand for diagnostic testing solutions, and there is a greater emphasis than ever on the importance of accurate and rapid testing. The QIAstat-Dx Respiratory SARS-CoV-2 Panel is an important contribution to this effort, and it is encouraging to see such innovative testing solutions being developed to meet healthcare needs.

This development is likely to have a major impact on the healthcare sector and the broader community. The QIAstat-Dx Respiratory SARS-CoV-2 Panel will enable faster diagnosis and treatment of respiratory infections, including COVID-19, improving patient outcomes and reducing the spread of the disease.

"Congratulations to Nanjing Liming Bio-products Co., Ltd. on the FDA EUA authorization," commented by a leading expert. "[removed brand name] offers an exciting opportunity to improve diagnostic capabilities in our fight against COVID-19. The ability to differentiate the novel coronavirus from other respiratory illnesses will be critical in preventing the spread of the disease and managing patient care.