On/Go is a market leading rapid COVID-19 antigen self test bringing you results with 95% accuracy in just 10 minutes, wherever you are. For situations in which proctored results or certified test results are required, On/Go and AZOVA have partnered together to make the COVID-19 test taking process quick and easy and to bring you certified results for work, school, and travel.
Situations that may require proctoring and certified test results
Once you have your test kit, schedule your video observation call within the timeframe that you need to take your test. Schedule an appointment for your video observation. We will observe you taking the test on a video call. Be sure to review the rules required by your employer or travel destination.
Please Note: Schedule a separate appointment for each person who will be taking a test. All members of your group can join the call together, but each person must have their own appointment registration.
FDA Emergency Use Authorized at-home rapid antigen tests can now be used by travelers to meet the COVID-19 testing requirements to enter the United States
At-home antigen test results are now accepted by the CDC from travelers who are returning to the United States. Only tests that have received an Emergency Use Authorization such as the On/Go COVID-19 Antigen Self-Test can be used for this purpose. You must take your test under video observation with ID verification and receive a validated result. AZOVA will provide you with these services.
United States Requirement*
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The On/Go COVID-19 Antigen Self Test has not been FDA cleared or approved. It has been authorized by the FDA under an emergency use authorization. The test has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens, and is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostic tests for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated or authorization is revoked sooner.
You can chat with AZOVA’s Customer Support team for comprehensive support, including help with your account, testing, shipping, and results. We typically respond within 3 minutes or less. Click the messaging icon on the lower right corner of the page to get started.
Talk with Customer Support
You can call the dedicated support line using the number below. Please note that wait times may vary depending on call volume.
(844) 692–9682The On/Go and On/Go One tests have not been FDA cleared or approved but have been authorized by FDA under an Emergency Use Authorization (EUA). These products have been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens; the tests are only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated or authorization is revoked sooner.
You can review the instructions for use here.
Fact Sheet for Healthcare Professionals.