Here's How We Help Your Employees




Here's How We Help Your Employees





What Medical Leaders Say About Rapid Testing

“Authorizing point-of-care serology tests [Rapid Antibody Tests] will enable more timely and convenient results for individuals who want to understand if they have previously been infected with the virus that causes COVID-19. Until today, serology test samples were generally only able to be evaluated in a central lab, which can be time consuming and use additional resources to transport samples and run the test.”
Dr. Stephen M. Hahn, M.D., 
FDA Commissioner

“Being immune means that if you’re exposed to the virus, your immune system will clear the virus out before it can establish a productive infection. So it’s really important from an epidemiological perspective to do these types of serology assays.”
Dr. Angela Rasmussen, Virologist at Columbia University in New York

"COVID-19 is still spreading rapidly throughout the United States, and antibody tests remain an underappreciated weapon in our fight to stop it. Armed with such tests, we can provide the public with much more specific information about their own susceptibility, possibly permit immune individuals to return to work, and help people make more informed decisions about when and whether to loosen restrictions on their social activities."
George Miller, Professor of pediatrics and epidemiology, Yale School of Public Health

"Ultimately, this might help us figure out who can get the country back to normal, people who are immune could be the first people to go back to normal life and start everything up again."
Florian Krammer, Professor in vaccinology, Mount Sinai's Icahn School of Medicine
  • 100% Sensitivity: No false negatives means you only send home those who should actually be quarantined
  • No waiting: Test results on-site in 10-15 minutes
  • No Medical Staff Needed: No medical staff needed. HR could administer the test in-house
  • Simple: As easy to do as a glucose test

  • ​Affordable:
     Test and retest as needed to make sure your business can stay open
  • Made In USA: Our lab wants to help get Americans back to work again, too!

The two most important facts to know:

1. Our test is 
made in the usa

Every step from Laboratory to Manufacturing is completed 
in Ohio, USA


FDA Registered Supreme Test: 

Sensitivity: 100% (NO false negatives)
Specificity: 99.2% (less than 1 false positive)

NEW: Oral Rinse PCR Test


Patient just rinses mouth with solution*, spits into vial, add stabilizer, seal and send to the lab.        

*Safe food grade if accidentally swallowed.


Does not need to be administered by a medical professional.                              

(Results in 24-48 hrs via secure portal.)


Contact us to develop your workplace COVID-19 testing solutions 
using Rapid Antibody Testing and PCR Testing.

We provide a solution, with NO false negatives* and less than 1% false positives. The BEST registered results for certainty in re-starting your business.

OUR PURPOSE: We’re committed to helping America get back to work. From Mom & Pop retail storefronts, restaurants, to manufacturing plants, safely re-opening is our priority. A fast, accurate, on-site test is the answer.

On April 1st 2020, governments began announcing ‘stay at home’ orders and it was clear the world would never be the same again.  
Our team set up a weekly Zoom call with a few colleagues, doctors, virologists, pharmacists and anyone we felt could help find a real solution. 

The result was this American-made,  totally accurate test which provides business owners and management with results in a record-breaking 15 minutes.

* "No false negatives" means you don't keep someone at work who might still be infected. If our test says Negative, they are negative. 



Our testing kits are proudly manufactured Ohio, USA

Restart YOUR BUSINESS with Confidence


"What I like about USA Rapid Test is the speed and the simplicity of the test. I also like knowing that the test is manufactured in the USA. This gives me peace of mind when questioning the reliability of the results. I like the idea that I can test my employees first thing in the morning before we have any patients in the office and 15 minutes later, I have the results." - B.H.
"USA Rapid Test has been helpful in getting some of our most vital employees back to work safely!" - E.K.
"Having the rapid testing in our office helped our patients feel confident that we were doing our part in the fight against COVID-19. It also helped us clear our staff of having COVID and in one case showed that her children that had tested positive for COVID now had the antibodies." - K.T.
"These tests completely handled the upset at our company with the COVID scare. We had all of our employees get tested and they felt much better knowing that they were in an environment that cared about their well-being and safety. My employees were actually more productive once they had this comfort." - L.B.

We can help you develop certainty on how to proceed. 
Protect your employees, their families and your company.

Still Have Questions?
Here Are Some Answers:

Just how accurate are the tests?

In over 700+ cases submitted to FDA, here's how our test performed:

  • Sensitivity: 100% - NO false negative results
  • Specificity: 99.2% - Less than 1% false positives
How fast can results be determined?

Results are visible in 10-15 minutes.  See the illustration above and the administering instructions included with the product data sheet in every box.  (Note: Results beyond 30 minutes are NOT VALID.)
When/why should I have an antibody test?

  • You or your health care provider believe you may have been exposed to the virus based on locations, of travel, your current or previous signs and symptoms (e.g., fever, cough, difficulty breathing).
  • You have been in close contact with an individual suspected of or confirmed to have COVID-19.

  • ​You want to verify worker wellness / ability to return to work.
Can I test my family and friends at home?

No.  This test is NOT approved for home use.
Do you have a video of how to perform the test?

How do I read the results?

We recommend engaging a phlebotomist to perform on-site delivery.  A total of four visually observable outcomes are possible, with the control (C) line appearing when sample has flowed through the cassette:

  • Positive Result, IgG and IgM: If the quality control line (C) and both detection lines (G) and (M) appear, then the novel coronavirus IgG and IgM antibodies have been detected and the result is positive for both the IgG and IgM antibodies.
  • Positive Result, IgM only: If both the quality control line (C) and the detection line (M) appears, then the novel coronavirus IgM antibody has been detected and the result is positive for the IgM antibody. This test detects IgM antibodies. IgM is usually the first antibody produced by the immune system when a virus attacks. A positive IgM test indicates that you may have been infected and that your immune system has started responding to the virus. When IgM is detected you may still be infected, or you may have recently recovered from a COVID-19 infection.
  • Positive Result, IgG only: If both the quality control line (C) and the detection line (G) appears, then the novel coronavirus IgG antibody has been detected and the result is positive for the IgG antibody. This test detects IgG antibodies that develop in most patients within seven to 10 days after symptoms of COVID-19 begin. IgG antibodies remain in the blood after an infection has passed. These antibodies indicate that you may have had COVID-19 in the recent past and have developed antibodies that may protect you from future infection.
  • ​Negative Result: If only the quality control line (C) appears and the detection lines (G) and (M) are not visible, then no novel coronavirus antibody has been detected and the result is negative.
Scientifically, how does the antibody test work?

The test strip contains a colloidal gold-labeled recombinant novel coronavirus antigen and quality control antibody colloidal gold marker, two detection lines (G and M lines) and one quality control line (C) fixed on a nitrocellulose membrane. M is fixed with monoclonal anti-human IgM antibody for detecting the novel coronavirus IgM antibody. G is fixed with monoclonal antihuman IgG antibody for detecting the novel coronavirus IgG antibody. The quality control antibody is fixed on the C line.
I'm a medical professional. Can you give me more technical info about the Rapid Test?

Our Rapid IgM-IgG Dual Antibody Test for COVID-19 is a lateral flow immunoassay used to qualitatively detect IgG and IgM antibodies of the novel coronavirus in whole blood. 
COVID-19 (Coronavirus) Antibody (Serology) Test: This is a blood test. It is designed to detect antibodies (immunoglobulins, IgG and IgM) against the coronavirus that causes the disease called COVID-19. Antibodies are proteins produced by the immune system in response to an infection and are specific to that particular infection. They are found in the liquid part of blood specimens, which is called serum or plasma, depending on the presence of clotting factors.
Can I test my employees at work?
Yes. (Most likely.)  Here are the CDC guidelines which encourage doing so for safety in the workplace.

Is your test "FDA Approved"?

Our test is FDA Registered and Authorized by the FDA to be delivered under the umbrella EUA (Emergency Use Authorization) for CLIA Level H Laboratories. It is an LDT (Laboratory Developed Test) which grants the authority to not require FDA Approval for use. “FDA Approved” is commonly misunderstood. There are 3 levels of FDA status to know:

  • FDA Approved:  There are ZERO COVID-19 tests that are actually FDA Approved. That process takes trials and usually 1-2 years of submissions to be completed.
  • FDA Authorized:  There are approximately 30 tests that have been Registered and then after closer review were given EUA Authorization for the time period of the pandemic. Those are the ones listed on their website. (Note: Many were given scrambled authorization and have now been removed.)  Additionally, this is where the EUA Umbrella Authorization falls. 
  • FDA Registered:  This means that a known entity, (ie: our laboratory is already a fully certified FDA Approved Facility) submits evidence of a tests science and results. The FDA then acknowledges, a small percentage who’ve received previous case approvals, with a case #, which ours has.
As note, for an FDA submission, the minmum required samples of standard results are 30. Our lab has submitted over 700 for our COVID Rapid Anitbody Test with Supreme Test scores of 100% Sensitivity and 99.2% Specificity – higher than anything else on the market.


(727) 441-3026

We're Here to Help 

Restart Your Business, Safely.

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