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Image: Abbott ID Now (Photo courtesy of Abbott)

Abbott Reissued FDA Emergency Use Authorization for ID Now COVID-19 Test

Abbott (Lake Forest, IL, USA) has been reissued Emergency Use Authorization (EUA) by the US Food and Drug Administration (FDA) for the company's ID Now COVID-19 test. More...
21 Sep 2020
Image: New Portable PCR COVID-19 Test Kit from Visby Medical Secures FDA Emergency Use Authorization (Photo courtesy of Visby Medical)

New Portable PCR COVID-19 Test Kit from Visby Medical Secures FDA Emergency Use Authorization

A new portable PCR COVID-19 test kit has been granted Emergency Use Authorization (EUA) by the US Food and Drug Administration (FDA) for use in lab environments. More...
18 Sep 2020
Image: SARS-CoV-2 emerging from the surface of cells (Photo courtesy of NIAID)

New CRISPR-Based Rapid Test Detects as Many Cases as Standard COVID-19 Diagnostic

A newly-developed CRISPR-based test has shown improved sensitivity and can detect nearly as many cases as the standard COVID-19 diagnostic. More...
18 Sep 2020
Illustration

FDA Publishes Comparative Performance Data for COVID-19 Molecular Diagnostic Tests

The US Food and Drug Administration (FDA Silver Spring, MD, USA) has published comparative performance data for some authorized COVID-19 molecular diagnostic tests. More...
18 Sep 2020
Illustration

Self-Swab COVID-19 Collection Kit Receives FDA EUA for Use by CLIA-Certified Laboratories

The Food and Drug Administration (FDA) has granted Emergency Use Authorization (EUA) to a new COVID-19 self-collection kit, enabling public health and large private labs to increase access to testing. More...
17 Sep 2020
Illustration

First-in-Class Rapid Diagnostic Test Measures COVID-19 Neutralizing Antibodies in Plasma and Serum

A new rapid diagnostic test is expected to be the market’s first COVID-19 rapid diagnostic test for measuring the levels of functional SARS-CoV-2 neutralizing antibodies in a lateral flow assay format. More...
17 Sep 2020
Image: The cobas SARS-CoV-2 & Influenza A/B Test (Photo courtesy of Roche)

Roche Granted FDA Emergency Use Authorization for Cobas SARS-CoV-2 & Influenza A/B Test

Roche (Basel, Switzerland) has received Emergency Use Authorization (EUA) from the US Food and Drug Administration (FDA) for a rapid version of its Cobas SARS-CoV-2 & Influenza A/B test. More...
17 Sep 2020
New
Gold Member
C-Reactive Protein Reagent
CRP Ultra Wide Range Reagent Kit
Automated Blood Typing System
IH-500 NEXT
New
FLU/RSV Test
Humasis FLU/RSV Combo
New
Auto-Chemistry Analyzer
CS-1200