Active Infection Test

Quest Diagnostics



Quest Diagnostics

Active Infection Test

This type of test helps to diagnose whether you currently have an active COVID-19 infection. A diagnosis can guide you and your doctor or healthcare provider to make an informed decision about self-isolating to protect your family and friends.

How to get tested:

Do you have a current COVID-19 electronic test order from your doctor? If so, click here. If not, you may be eligible to receive $0 out-of-pocket COVID-19 testing with most insurance and federal programs. You can also purchase a drive-up or at-home kit through QuestDirect.

Who can get tested:

Active infection testing may be right for you if you are currently experiencing SARS-CoV-2 (COVID-19) symptoms or were exposed to the virus in the last 14 days. Common COVID-19 symptoms include fever, cough, and shortness of breath. This test may also be right for you if you need COVID-19 testing to meet school, work, or travel requirements.

How the test works:

Your doctor or other healthcare provider will collect a sample through a nasal or throat swab. You can also opt to collect a sample yourself with drive-up or at-home options from QuestDirect. The sample is then sent to Quest laboratories for processing.

Getting test results through MyQuest

If you receive a Quest COVID-19 test, your test results can be sent to you automatically through the secure MyQuest online portal. This is usually the quickest way to get results.

Don’t have MyQuest?
Sign up now to get your COVID-19 test results online.

Launch MyQuest

Get MyQuest Instructions
Choose language:

MyQuest App

COVID-19 testing statements

  • The antibody tests and the molecular tests (together “All tests”) have not been FDA cleared or approved;
  • All tests have been authorized by FDA under EUAs for use by authorized laboratories;
  • The antibody tests have been authorized only for the detection of IgG antibodies against SARS-CoV-2, not for any other viruses or pathogens;
  • The molecular tests have been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses, pathogens; and,
  • All tests are 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 authorization is terminated or revoked sooner.