COVID-19 company Meenta on Tuesday announced a partnership with Mirimus to provide the K-12 schools across the US with easy access to affordable clinical testing using a HIPAA-compliant, secure API integration and dashboards that turns data into actionable insights.
Mirimus has developed a COVID-19 testing platform (SalivaClear) which enables saliva-based sampling, pooled testing and individual diagnostics with just one sample from each individual. This K-12 COVID-19 testing programme is available immediately on the Meenta Marketplace, a testing marketplace that provides schools access to millions of tests from different clinical labs and diagnostic companies.
Using Mirimus' SalivaClear technology, each tube has a unique barcode that is scanned before saliva samples are collected on site and sent directly to the lab, where samples are pooled in batches of 24 samples and tested. These results are sent back to the school within 24 hours of the lab. Positive pools are re-tested in sub-pools of two samples and then individually tested if they test positive again.
The partners added that SalivaClear enables high-quality, simple, and cost-efficient detection of SARS-CoV2 to quickly isolate COVID-19 hotspots before they can become outbreaks. This approach is a highly accurate, RT-PCR-based testing strategy based on leading research from Yale University and is operating under an Emergency Use Authorization from the US FDA.
MaaT Pharma reveals positive 18-month data for MaaT013 in GI-aGvHD
Innate Pharma advances Sanofi-developed NK cell engager to Phase 2 for blood cancer patients
Precision Epigenomics partners with TruDiagnostic
Illumina's GRAIL divestment plan receives EC approval
Soligenix receives orphan drug designation from FDA for active ingredient in SuVax
Candel Therapeutics granted FDA Orphan Drug Designation for CAN-2409 in pancreatic cancer treatment
Lipogems completes patient enrolment in ARISE I US FDA IDE study
Amylyx Pharmaceuticals' AMX0035 shows promising impact on Wolfram syndrome symptoms
Ondine Biomedical's Steriwave approved for use by HCA UK
Roche attains CE Mark for first companion diagnostic for HER2-low metastatic breast cancer
Cadrenal Therapeutics' tecarfarin receives US FDA Orphan Drug Designation
BioCity Biopharma's BC2027 Phase one study IND application receives US FDA approval
Seres Therapeutics completes patient enrollment for SER-155 Phase 1B trial
Syros receives Fast Track Designation from FDA for tamibarotene in AML