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Guidance for SARS-CoV-2 Point-of-Care Testing



How to navigate through covid

Point-of-care tests, such as some rapid tests for diagnosing an infectious disease, provide results within minutes of the test being administered, allowing for rapid decisions about patient care. POC tests can also extend testing to people residing in communities who cannot readily access care.


POC tests are used to diagnose current or detect past SARS-CoV-2 infections in various settings, such as:


  • Physician offices

  • Urgent care facilities

  • Pharmacies

  • School health clinics

  • Long-term care facilities and nursing homes

  • Temporary locations, such as drive-through sites managed by local organizations


Summary: This CDC Web resource provides guidance on the regulatory requirements for SARS-CoV-2 POC testing, using POC tests safely, and information on reporting POC test results.


Regulatory Requirements for POC Testing


Who can do POC testing?

Sites that perform POC testing are required to have a Clinical Laboratory Improvement Amendments (CLIA) certificate (see this brochurepdf iconexternal icon). There are four different types of CLIA certificates, any one of which is appropriate for POC testing. See this Centers for Medicare & Medicaid Services (CMS) documentpdf iconexternal icon that describes the different types of CLIA certificates.


A CLIA Certificate of Waiver is appropriate for POC testing and can be obtained as follows:


  • Complete an application, available on the CMS CLIA website or from a local State Agency

  • Send the completed application to the address of the local State Agency for the state where testing will be performed

  • Pay the CLIA Certificate of Waiver fee, following instructions provided by the State Agency


See How to Obtain a CLIA Certificate of Waiver icon for more information. POC testing can be performed after the laboratory or testing site has received a CLIA certificate number.


The laboratory or testing site must keep its certificate information current. The State Agency should be notified of any changes to the laboratory or testing site ownership, name, address, or director within 30 days.


What tests can be used for POC?

See the US Food and Drug Administration (FDA) website for a list of the SARS-CoV-2 POC tests that have received Emergency Use Authorization (EUA)external icon. Tests that have been authorized for use in a POC setting will have a W, for Waived, in the Authorized Settings column of the FDA table.


The laboratory or testing site must use a test authorized for POC use by FDA and must follow the manufacturer’s instructions for each POC test. The instructions for use provide specific information on how to perform the test, which specimens can be used, and the people who may be tested.


All of the FDA-authorized tests for current SARS-CoV-2 infection are for use on symptomatic people. However, CMS has indicated that CLIA will temporarily allow CLIA laboratories and other CLIA testing sites to use SARS-CoV-2 POC antigen tests on asymptomatic people for the duration of the COVID-19 public health emergency.


For more information and additional resources for POC testing, see CDC’s Waived Tests Web page.


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