Diazyme Laboratories
Business Services · California, United States · 11-50 Employees
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Overview
Headquarters
12889 Gregg Ct, Poway, California, 92064...Phone Number
(858) 455-4768Website
www.diazyme.comRevenue
$15.9 MillionIndustry
About Diazyme Laboratories
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Diazyme Laboratories is experiencing very low activity levels compared to other companies in the Business Services sector.
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Diazyme Laboratories Tech Stack
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Diazyme Laboratories News & Media
Diazyme Laboratories, Inc. Acquires Carolina Liquid Chemistries Corp.
Diazyme acquires Carolina Liquid Chemistries, expanding FDA-registered diagnostic reagents and chemistry systems to enhance lab testing solutions.Glycated Albumin Assay Market is Projected to Potential at a 7.7% CAGR by 2028 | Diazyme, LifeSpan BioSciences
SEATTLE, UNITED STATES, UNITED STATES, January 7, 2022 /EINPresswire.com/ -- New Research Study "Glycated Albumin Assay Market Market 2022 analysis by Market Trends (Drivers, Constraints, Opportunities, Threats, Challenges and Investment …Diazyme Laboratories, Inc. Announces CE-IVD for its Semi-Quantitative SARS-CoV-2 Neutralizing Antibody Test
SAN DIEGO, April 01, 2021 (GLOBE NEWSWIRE) -- Diazyme Laboratories, Inc. announced March 30th that it has obtained CE-IVD marking for its SARS-CoV-2 neutralizing antibody test. The Diazyme test is a high throughput chemiluminescent immunoassay with excellent correlation to a fluorescence based neutralization assay, which has been used to evaluate the adaptive immune response in vaccine studies1. Diazyme also announced plans to work with US FDA for EUA application.Diazyme Laboratories, Inc. Receives Reissued EUA for Semi-Quantitative SARS-CoV-2 IgG Test
SAN DIEGO, March 23, 2021 (GLOBE NEWSWIRE) -- Diazyme announces that it has received a reissued Emergency Use Authorization (EUA) for its Semi-Quantitative DZ-Lite SARS-CoV-2 IgG CLIA test which is run on the fully automated DZ-Lite 3000 Plus chemiluminescence analyzer. The FDA has already granted Diazyme an EUA for its qualitative DZ-Lite SARS-CoV-2 IgG CLIA test (July, 2020). Upon reviewing additional data, the FDA has authorized the Diazyme IgG assay to be used as a
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