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4 news found

FDA Authorizes New High-Throughput, Automated System for Leading COVID-19 Test

FDA Authorizes New High-Throughput, Automated System for Leading COVID-19 Test

Amplitude Solution with TaqPath COVID-19 High-Throughput Combo Kit enables labs to scale high-sensitivity PCR testing The Amplitude Solution enables clinical and public health laboratories to scale gold standard PCR testing and process up to 8,000 samples in a single day with minimal staffing resources and a secured supply of kits, reagents and ...

ByThermo Fisher Scientific, LIMS & Laboratory Software


Sherlock Biosciences Receives $5 Million Grant to Advance INSPECTR™ Platform for COVID-19 Self-test

Sherlock Biosciences Receives $5 Million Grant to Advance INSPECTR™ Platform for COVID-19 Self-test

“In addition to advancing our INSPECTR platform development to be as sensitive as gold-standard PCR tests, the funding will support our development of an over-the-counter disposable product, similar to an at-home pregnancy test, that can be used to detect SARS-CoV-2, the virus that causes COVID-19. ...

BySherlock Biosciences, Inc.


MiraDx Offering COVID-19 PCR Testing for California Skilled Nursing Facilities

MiraDx Offering COVID-19 PCR Testing for California Skilled Nursing Facilities

The MiraDx lab, which is now exclusively processing COVID-19 tests, has capacity of up to 5,000 tests per day for SNFs to ensure they are able to comply with the state’s guidelines, which include: exclusive use of PCR testing with 48-hour turnaround time; baseline testing for all residents and healthcare personnel in ...

ByMiraDx


QIAGEN HPV DNA test donation to expand access to cervical cancer screening for women in rural India

QIAGEN HPV DNA test donation to expand access to cervical cancer screening for women in rural India

QIAGEN"s current "gold standard" HPV test platform - the digene HPV Test - uses advanced molecular diagnostic technologies to identify the presence of the genetic code (DNA) of the key high-risk, cancer-causing types of HPV. In the U.S., it is approved to be used together with a Pap test in women 30 years and older. In Europe it ...

ByCSRwire - Corporate Social Responsibility Newswire

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