COVID-19 Testing for Corporations
Deploy Simple and Convenient COVID-19 Testing Today
FDA EUA Authorized, Simple Saliva Kit, No Nasal Swabs Needed
How It Works:
Create Testing Program
We work with HR to analyze your risk across your population based on many factors including location, density, type of work environment, demographic, health history and we provide a regiment of testing to reduce your risk while minimizing testing cost.
Test Your Employees
1Health.io will provide the test kits to their location and if required validate that the sample was collected by the employee over video link
Receive Their Results
Test results will be delivered to the employee and designated care providers or HR on approval by the employee.
Receive Weekly Reports
Weekly reports provide visibility to HR on number of employees tested, rate of infection over time and other data sets.
Putting HR Back In Control
We have a testing process to help HR get control over infection in their workforce. Our team will help you analyze your risk factors and the frequency and type of testing needed to get your workforce back to work while minimizing the risk of infection.
HR can decide who should be supervised during sample collection over video link, ensuring correct collection of saliva sample by the employee.
Noninvasive And Simple Collection Method
We use a simple and effective saliva collection method. This method enables the employee to self collect their sample without the involvement of healthcare provider.
Trusted Healthcare Platform
Trusted healthcare platform that powers testing for large health and wellness brands.
Simple weekly reports on who has been given the test, who has completed the test and rate of infection across the larger employee population.
Your employee decides how their results are shared with their physicians or other care providers and corporate HR.
The First FDA EUA Authorized
At-Home Saliva COVID-19 Test
Our self-collection testing kit for COVID-19 uses a hassle-free saliva sample to determine if your employees are infected with the SARS-CoV-2 virus. We’ve partnered with labs operating under the Emergency Use Authorization guidelines issued by the FDA. Our test kits include a complimentary express priority return mailer for sending the sample to the lab. Within 72 hours of the lab receiving the sample, you will be faxed the result and the employee can access the result in their dashboard. If the result is positive, it is reported to appropriate authorities.
Saliva Collection Tube
Digital Results Available Within:
72 hours of the lab receiving the sample
Sensitivity 99.99% Specifity (%) 100%
This test has been authorized by the FDA under an Emergency Use Authorization for use by authorized laboratories. This test has not been FDA cleared or approved. This test has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens. This test 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 Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.