COVID-19
Sample Collection

Simple and Comfortable Sample Collection.

The GENETWORx COVID-19 Nasal Swab Test Kits come with all the necessary instruments and clear instructions for collecting samples. The sample should be sent back the same day it is collected so GENETWORx can get you the accurate, timely results you need

With GENETWORx, Self-Administered COVID-19 Test Kits can be Received at Homes, Offices and Dorms

GENETWORx is your one stop solution for COVID-19 testing. We now offer COVID-19 nasal swab self-collection test kits, in addition to on-site testing and COVID-19 management software. The GENETWORx COVID-19 Nasal Swab Test Kit enables your employees, students, residents and patients to collect a sample at home, send it to the lab, and receive convenient, accurate, and timely COVID-19 diagnostic test results. It is both simple and convenient. A qualified healthcare provider (such as physician, nurse practitioner, or physician’s assistant) is required to order test kits and provide any necessary follow up.

Order GENETWORX COVID-19 Nasal Swab Test Kits Today

The GENETWORx COVID-19 Nasal Swab Test Kit is approved for adults age 18 and older

99% Accurate Test Results

Testing without accuracy does not help anyone. The GENETWORx PCR COVID-19 Nasal Swab Test Kit is 99% accurate. We supply thousands of at-home test kits to universities, employers, and organizations, and can have test kits out the door to your population within hours.

GENETWORx is committed to re-opening America safely so people can go back to work, live on campus, attend school in-person, have loved ones visit them in hospitals and nursing homes, play sports safely, travel for leisure or work, and much more. Providing the ability for people to conveniently take accurate, rapid result COVID-19 tests at home is another example of our commitment to America during this pandemic.

Our Partners Include:

Ways to partners with us

Full Service:

Complete end-to-end administration.

Self Service:

We train and provide tests, you administer.

Self Collection:

At home testing for employees.

Order GENETWORX COVID-19 Nasal Swab Test Kits Today

The GENETWORx COVID-19 Nasal Swab Test Kit is approved for adults age 18 and older

FAQs for organizations

Yes, the GENETWORX COVID-19 diagnostic test kits for at-home use have received Emergency Use Authorization (EUA) from the FDA.

Ordering organizations receive an invoice with net 15 payment terms upon order.

The GENETWORX COVID-19 at home-test kit cost includes the test kit, shipping the kit to the recipient and back to the lab, lab processing, results delivery and lab reports.

Yes! Test kits can be sent to each recipient’s address, a central location, or a combination of the two.
In partnership with Nucleus, GENETWORx provides customers Aura, a unique software which is a total end to end digital management and medical data system. With the Aura app, GENETWORx customers receive their test results on their mobile devices, and can download their lab reports. In addition, Aura provides organizations the ability to share on-site test locations, schedule tests, collect daily symptom tracking inputs, conduct contact tracing and access dashboards regarding all aspects of testing and test results at their fingertips.
To process tests GENETWORx must receive an order from a physician or other qualified healthcare provider, similar to the requirement for a prescription for some medications. We can work with your organization’s physician or other healthcare provider. If needed, GENETWORx can help you choose an appropriate healthcare provider to order tests

This test has not been FDA cleared or approved, but has been authorized for emergency use by FDA under an EUA for use by authorized laboratories; This test has been authorized only for the detection of nucleic acid from SARS-CoV- 2, not for any other viruses or pathogens; and The emergency use of this test 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, Medication, and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated or authorization is revoked sooner.

For more information on our testing capabilities or for instructions on the gathering of samples, please contact GENETWORx by: