Make Smarter Decisions for your Business and Employees with On/Go™

For employers of all sizes, schools and governments, On/Go provides our rapid antigen testing and technology to deliver real-time results and proactive population management. On/Go powers targeted interventions, making managing outbreaks simpler and more effective.  On/Go is the easiest way to ensure your organization is compliant with the new OSHA mandates.

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is a solution like no other

Our AI-powered COVID-19 solution connects rapid testing with the real-time data you need to make the best decisions for your business and employees. On/Go provides fast, accurate and actionable results in the first end-to-end "Testing-to-Tracing COVID-Control" solution.

What is the
On/Go Population Management Platform?

Our AI-powered platform seamlessly integrates with On/Go rapid tests, offering a real-time solution to avoid costly shutdowns through rapid, targeted interventions. To support the fight against COVID-19, our portal provides:

  • Live tracking and viewing of results, by individual or cohort
  • Protocol engine to define groups, routines and interventions
  • Integrated communications to manage messages to individuals or teams

We are excited to offer a smarter COVID solution that enables healthier, happier citizens, an open economy and enhanced peace of mind.

As COVID evolves, so do we.

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The On/Go Technology

Our COVID Testing Platform

The On/Go testing-to-tracing solution delivers rapid test results, tracks your testing history, and lets your teams easily share results with those who need to know.

Learn about the On/Go Tech

On/Go for My Family

Get Back to What Matters

On/Go is a solution like no other.  By connecting testing with real-time data to keep track of your family and their current status, you'll know you are ready to embark together on the next family vacation, take your child to his/her sporting events, or just be confident when you are visiting your loved ones.

On/Go for my family and me


This product has not been FDA cleared or approved but has been authorized by FDA under an Emergency Use Authorization (EUA). This product 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 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.