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Our solution is the first all-in-one COVID-19 solution that combines our FDA authorized, best-in-class rapid self-tests with cutting-edge technology to help protect students, faculty and families.
For schools, universities and summer camps of all sizes, On/Go provides an affordable, easy and data-driven way to return to in-person activity as uninterrupted as possible. With On/Go, we help you maintain a safe and healthy environment for those in your care.
Our model, called Diagnostics as a Service (DaaS), offers a seamless combination of testing and technology to help control COVID. From easy onboarding to market-leading rapid tests delivered straight to the home, to post-diagnosis resources, we take care of you from testing to care.
Our AI-powered platform provides real-time COVID test results that give you the precise knowledge to act immediately. With our solution, you can quickly implement targeted, data based interventions based on real-time data, customizable to your organizations' needs.
Get tests quickly shipped to individuals' homes, or provide testing on site. Within minutes of taking a test, your school population will know their results and can act accordingly.
We're here to support you every step of the way. From account setup to proctoring services to COVID testing results management, we'll make sure you can quickly get your organization up and running on our platform.
Whether you're looking for something to have on hand or for something that fits in the palm of your hand, the On/Go and On/Go One rapid COVID-19 antigen self-tests and companion app make testing quick, simple and portable. For those at home and those on the go. On/Go and On/Go One are there for you!
For in vitro diagnostic use only. Must be age 2+ to use these tests.
Learn more about On/Go One and On/Go.
Our top-rated iOS and Android mobile app delivers an intuitive testing experience. With over 30,000 five-star reviews, the On/Go app provides rapid test results, tracks your testing history and lets you easily share results with those who need to know.
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The 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.
The On/Go COVID-19 Antigen Self Test and the On/Go One COVID-19 Antigen Home Tests are lateral flow chromatographic immunoassays intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in anterior nasal swab specimens directly from individuals within 7 days of symptom onset or without symptoms or other epidemiological reasons to suspect COVID-19
