We have written at length about the U.S. Food and Drug Administration’s (FDA’s) actions to promulgate regulations specifying the agency’s authority to regulate laboratory developed tests (LDTs) as ...
New cost-effective method for collecting DNA specimens from oral and other biological fluids and tissue PORTLAND, Ore.–(BUSINESS WIRE)–August 13, 2014– Sedia Biosciences Corporation announced today ...
CHEYENNE, WY / ACCESSWIRE / February 24, 2021 / MJ Biotech, Inc. (OTC PINK:MJTV), is pleased to report that Sterile and individually wrapped FDA approved nasopharyngeal (nasal) specimen collection ...
SAFER™ Sample Kit offers accessible, non-invasive, and safe sample collection via saliva to enable cost-effective mass testing; Proprietary reagent inactivates virus in sample, while keeping sample ...
Enables CLIA-certified laboratories using HealthPulse@home authorized labeling instructions to offer new test kits under Audere's EUA HealthPulse@home provides a faster, less expensive, hassle-free ...
NEW YORK, NY, April 21, 2021 (GLOBE NEWSWIRE) -- Enzo Biochem, Inc. (NYSE:ENZ) (“Enzo” or the “Company”), a leading biosciences and diagnostics company, today announced that the Food and Drug ...
Phoenix, AZ, March 16, 2020 (GLOBE NEWSWIRE) -- via NEWMEDIAWIRE -- No Borders, Inc. (OTC:NBDR) today announced the launch of its “MediDent Supplies Covid-19 Home Specimen Collection Kit” to support ...
Data Bridge Market research released a new market study on Specimen collection kit with 100+ market data Tables, Pie Chart, Graphs & Figures spread through Pages and easy to understand detailed ...
CHICAGO — The use of a lymph node specimen collection kit during non-small cell lung cancer resection significantly improved staging quality and OS, according to data presented at ASCO. The American ...
ST. PETERSBURG, Fla. — COVID-19 specimen collection kits are of high importance, but in short supply right now across the country. Counties here in Florida are feeling the effect. Test sites in ...
This Client Advisory addresses some frequently asked questions for SARS-CoV-2 diagnostic test developers and provides an overview of recent updates relating to Emergency Use Authorizations (EUAs) ...
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