LabCorp has achieved a milestone as the initial company granted permission to market its COVID-19 test kit directly to consumers without requiring a doctor's prescription, as detailed in a company announcement.

As one of the nation’s leading diagnostic testing organizations, LabCorp is poised to be a strong contender against businesses such as EverlyWell, which obtained approvals for its home testing solutions in May; MyLab Box, which recently revealed a collaboration with Walmart to distribute COVID-19 test kits through the retailer; and LetsGetChecked, offering its own at-home testing option.

LabCorp originally secured the first FDA approval for its test kit, and this new authorization now enables the company to distribute the product via retail outlets without a prescription requirement.

“We are providing individuals with the ability to gain insights into their health and make well-informed choices with the first FDA-authorized over-the-counter at-home collection kit for COVID-19,” stated Dr. Brian Caveney, chief medical officer and president of LabCorp Diagnostics, in a press release. “This authorization will allow us to facilitate broader access to testing, help limit the transmission of the virus, and contribute to the well-being of our communities.”

Any measure that simplifies the process for individuals to be tested for SARS-CoV-2, the virus responsible for COVID-19, is undoubtedly beneficial. This development also aligns with a wider movement to enhance healthcare accessibility for consumers with the goal of lowering expenses.

Upon acquiring the COVID-19 test kit, customers complete registration on the company’s website and subsequently adhere to the provided guidelines. Test outcomes are communicated through a secure online platform, and a medical professional is accessible to guide individuals who receive a positive result regarding appropriate treatment options.

The company emphasizes that its kit should not replace consultations with a healthcare provider and is designed for use by individuals aged 18 years and older.

It is crucial to understand that the LabCorp PCR test has not received standard FDA clearance or approval and is currently being offered under an Emergency Use Authorization.