RETURNING TO WORK WITH CONFIDENCE
Rapid Testing Removes Fear
• Results in 15 mins!
• No Waiting
• No Painful Swab
• No Doctor Visit
• Test On Location
• No Waiting
• No Painful Swab
• No Doctor Visit
• Test On Location
Simple Protocols to Keep Your Business Open Safely
The two most important facts to know
about our COVID-19 Tests:
1. Our testS ARE
made in THE usa
Every step from Science in Massachusetts to Manufacturing and Laboratory in Ohio,
is completed in the USA.
is completed in the USA.
2. Our testS ARE
HIGHLY ACCURATE
FDA Registered Supreme Test:
Sensitivity: 100% (NO false negatives)
Specificity: 99.2% (less than 1 false positive)
Sensitivity: 100% (NO false negatives)
Specificity: 99.2% (less than 1 false positive)
No Refunds or Exchanges.
USA Rapid Test CEO on FOX Business
Why is Disney World open and Disneyland closed?
What is the 4th "W" for the
US Surgeon General?
What is the 4th "W" for the
US Surgeon General?
Antibody Test Results in 15 Minutes
Rapid Antibody Testing is Quick, Easy and Reliable
Our Test Kits provide the most accurate on-site solution you can use to quickly and cost-effectively
return your employees to work; with results in only ten to fifteen minutes. Know, before you go!
The simple procedure and results are illustrated below.
No Refunds or Exchanges.
Medical Leaders in the News on 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 [IgG positive] 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
New: Oral Rinse
PCR Test
NO INVASIVE SWAB!
The Quiksal® Oral Rinse Specimen Collection Device is designed to replace nasal swabs and saliva collection. A 2ml oral rinse* that is swished for 60 seconds
and returned to its container.
*Safe food grade if accidentally swallowed.
An FDA EUA covers the Quicksal® Oral Rinse Collection Device. Viral collection methods for PCR testing of COVID-19 have traditionally used a swab or saliva technique.
Nasopharyngeal swabs are typically considered the gold standard for sensitivity however the inherent
drawbacks of improper specimen collection and the invasive nature of the swab negatively impact the patient
experience and validity of testing. The use of a shallow nasal swab or saliva collection techniques is
significantly less invasive however is not as effective at gathering a valid specimen.
USA Rapid Test and RevolutionDx (CLIA# 36D2158721, COLA# 29299) want to introduce your laboratory
to a superior viral collection device that is easier to use and less invasive than traditional testing.
An FDA EUA covers the Quicksal® Oral Rinse Collection Device. Viral collection methods for PCR testing of COVID-19 have traditionally used a swab or saliva technique.
Nasopharyngeal swabs are typically considered the gold standard for sensitivity however the inherent
drawbacks of improper specimen collection and the invasive nature of the swab negatively impact the patient
experience and validity of testing. The use of a shallow nasal swab or saliva collection techniques is
significantly less invasive however is not as effective at gathering a valid specimen.
USA Rapid Test and RevolutionDx (CLIA# 36D2158721, COLA# 29299) want to introduce your laboratory
to a superior viral collection device that is easier to use and less invasive than traditional testing.
Still Have Questions?
Here Are Some Answers
How accurate are the Rapid Antibody Test results?
Performance is measured by the Supreme Test: Our test has displayed these standardized results in over 700+ cases submitted to FDA. Our Genetic Laboratory partner performs daily quality-control validations.
- Sensitivity = 100% - Should register NO false negative results.
- Specificity = 99.2% - Per 100 test samples a less than 1% false positive rate.
How fast can the Rapid Antibody Test results be determined?
Results are visible in 10-15 minutes after sample and buffer are combined in the cassette sample well. The C (Control) line must appear and ANY appearance of a G or M line, even if faint is a result. For interpretation direction, 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.
Can I COVID Test test my employees at work?
Most likely, yes. Here are the CDC guidelines which encourage doing so for safety in the workplace.
Can I test my family and friends at home?
No. This test is NOT for home use, is not recommended or approved for home use or outside the supervision of the laboratory.
How do I read the Rapid Antibody Test 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:
- Result, IgG and IgM: ACTIVE VIRUS - 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. Have patient/employee get PCR definitive test.
-
Result, IgM only: ACTIVE VIRUS - 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.
-
Result, IgG only: IMMUNITY - 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: CLEAR - 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.
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.
-
Your employer wants to verify wellness to return to work.
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.
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.
Do you have a video of how to perform the test?
Why 'No Refunds or Exchanges'?
Once product has left our warehouse, we can no longer attest to the temperature of storage, tampering and other factors. This is mandated due to the medical nature of these products being under laboratory supervision. (The only exception would be if we're notified PRIOR to shipping.)
No Refunds or Exchanges.
WHAT CLIENTS HAVE TO SAY...
Chiropractor
"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.
Manufacturer
"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.
Meet Our Management Team
On April 1st 2020, governments began announcing ‘stay at home’ orders and it was abundantly clear the world would never be the same again. Our team set up a weekly Zoom call with a few colleagues, doctors, virologists, pharmacists, politicians and anyone we thought could be part of the solution. The call attracted several hundred professionals from around the world. It began with discussion of preventative measures and the quest for a remedy or vaccine. Soon, with the pandemic having no end in sight, the demand for testing solutions was paramount. We went into action and set-up a line with multiple distributors and resellers to streamline access to our US only supply chain as quickly as possible.
David lee jensen
Our CEO is a 2-time Bestselling Author, speaker, and serial entrepreneur who started this venture with the purpose of helping recover our country's productivity and economy.
monica agami
Our COO is a successful businesswoman who owns a Certified Financial Planning firm that she built. Now she's added helping her peers get back to business safely.
sunny jensen
Our CFO and VP of Quality Service is a seasoned executive who creates stability for our organization by ensuring we deliver the highest quality products.