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How you collect nasal swab makes a big diagnostic difference. 


RT-PCR testing is the gold standard with the highest accuracy on the market. These tests have a 98-99% sensitivity (meaning 98-99% of positive tests are correct) and a 99% specificity (meaning 99% of negative tests are correct). Our FDA authorized test kits have received Emergency Use Authorization for at home, in office, or in-pharmacy self-administration. You will take the test and the test kit back to one of our CLIA certified lab partners. This test kit uses the painless anterior nasal swab where you swab the inside of your nostrils and not a deep swab. This mitigates any risk of exposure for all downstream processes and eliminates the need for UN3373 biohazard shipping designation with clearance from USPS, FedEx, & UPS.


Preservation formulation is able to identify viral RNA infections at their earliest stage from as few as 200 copies/ul (lateral flow rapid antigen tests need 10,000-20,000 copies/ul). Viral RNA samples maintain the highest bio-sample efficacy with well over two weeks post-collection stability for optimal testing accuracy. In addition, samples require no special temperature-controlled storage or transport.


  • Formulation identifies infections at its earliest stage from as few as 200 copies/ml (lateral flow rapid tests need 10,000-20,000 copies/ml)
  • 100% Inactivation of the live virus within the device at ambient temps
  • Mitigates any risk of infection throughout the testing process
  • Non-invasive & painless collection maintaining critical biosample consistency
  • Delivers 99.998% highest levels of testing accuracy & sensitivity
  • Single device for DNA & viral RNA applications
  • No post-collection temperature-controlled storage or transport of saliva samples
  • Well over 10 days of post-collection stability with no degradation in sample efficacy
  • Formulation provides safe, immediate testing with no hood containment
  • Process numerous tests from a single saliva sample
  • Shipping clearance from USPS, FedEx, and UPS eliminating UN3373 sample designation
  • Pinpoint life-cycle stage of active viral infection
  • Mass-testing scalability & easy device integration using validated and supported processes

At Home Self-Collected Nasal Swab Sample

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