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Welcome to Anytime Covid Test

Order Your Covid-19 Rapid Test Today!

Results in 15 Minutes or Less in the privacy of your home.  No waiting on labs

Priority Shipping Notice: Due to Covid-19 Shipping Providers including the USPS (United States Postal Service), UPS and FedEx no longer guarantee expedited services.  We will continue to ship priority and provide tracking.  After order submission, no cancellations or refunds will be made.

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At Home Covid-19 Antibodies Rapid Test
No Doctor Office or Lab Visit Needed

Anytime Covid Test, LLC is working with individuals, community organizations, employers, groups and agencies to offer an at home pre-screening test for COVID-19 antibodies that gives private and confidential results in 15 minutes or less in the privacy of your home or office. This test helps to determine whether you have been exposed to the virus within the past 4 to 24 days. This rapid test cassette reliably identifies IgG and IgM antibodies specific to SARS-CoV-2 in a sample of blood drawn with a finger prick, without exposing yourself to this or other viruses with an unnecessary trip to the lab, doctors office or field visit.


COVID-19 is thought to spread mainly through close contact from person-to-person.  Some people without symptoms may be able to spread the virus. We are still learning about how the virus spreads and the severity of illness it causes.

Important:  In the event you get a positive test result, we will schedule a one on one call with our doctor to discuss next steps at no additional charge.

Confidential Results in 15 Minutes or Less!
​No Doctor Office or Lab Visit Needed


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About Screening

for COVID-19

Anytime Covid Test, LLC via Clungene's Pre-Screening Covid-19 test has not been FDA cleared or approved, The FDA is allowing Clungene® SARS-CoV-2 IgG/IgM Rapid Serology Test to be made available under its new policy dated May 4, 2020.  This FDA authorization is commonly referred to as an Emergency Use Authorization (EUA). As required, the completed template and associated documentation were submitted on May 15, 2020 and are waiting feedback from FDA. The submission (EUA#201121) included updated validation reports and additional clinical data. Clungene’s establishment registration & device number on the FDA’s website is  3‍0‍0‍9‍4‍1‍4‍5‍4‍6. Under the Emergency Use Authorization (EUA), this test is used only for the possible detection of SARS-CoV-2, (COVID-19) not for any other viruses or pathogens. Anytime Covid Test, LLC is providing this test based on tests developed from various manufacturers and providers.


Such tests have either received an emergency use authorization (EUA) from the U.S. Food and Drug Administration (FDA) or are in the process of applying for an EUA from the manufacturers or were released for use under FDA guidance, “Policy for Diagnostic Tests for Coronavirus Disease-2019 during the Public Health Emergency - Immediately in Effect Guidance for Clinical Laboratories, Commercial Manufacturers and Food and Drug Administration Staff” that was updated on May 4, 2020.  Tests being performed under an EUA have not been FDA cleared, approved or received independent validation of these tests.  In addition, various manufacturers have submitted or are in the process of applying for EUA for their test.