Emergency Use Authorization

HealthTrackRx is one of twenty–seven labs to hold an FDA EUA for COVID–19 testing. As a condition of authorization, we are required to clearly state the use of our authorized product, described below:

  • This product has not been FDA cleared or approved by FDA, but has been authorized by FDA under an EUA for use by authorized laboratories;

  • This product 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 product 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 Act, 21 U.S.C. § 360bbb–3(b)(1), unless the declaration is terminated or the authorization is revoked sooner.

PATIENT FACT SHEET

HEALTHCARE PROVIDER FACT SHEET