COVID Community Testing 

**Note before your appointment you

MUST create a patient profile at:


Three steps to COVID Testing

Step 1

Schedule an appointment

Remember where you scheduled your appointment you will need the name of your test site location for the next step.


Schenectady and Washington County are offering walk-in testing. To find more information on testing in those counties, click the links below.

*If testing with the Clarifi COVID-19 Saliva Test, please follow the next two steps.


Create a profile

Organization Type: Community Testing

Organization: Enter the name of the testing location where you scheduled your appointment from the previous step. 

You will have to create a profile before you can be tested!!


Get tested

Read through the information below, there are some important steps you must follow before getting tested with the Clarifi COVID-19 Saliva Test!

What you need to know before your appointment



ONE HOUR BEFORE TESTING: Do not brush your teeth or use mouth wash. 

30 MINUTES BEFORE TESTING: Do not eat or drink anything, this includes gum, mints, lozenges, etc.

30 MINUTES BEFORE TESTING: Do not smoke, vape or use smokeless tobacco products.  

BEFORE ARRIVING: An account must have been created at 

BRING: Legal/valid identification and insurance cards

PCR TEST: This is not a rapid test, this is a PCR test you will receive your test results within 24-48 hours of receipt at Quadrant Laboratories.  You will be notified by email when your results are ready to be viewed in your patient profile. 

Once you arrive at your appointment

CHECK-IN:  staff will assure you've created your COVID-19 patient profile at 

TEST REGISTRATION:  The staff will ask you a series of questions (listed to the right) before self-administering the COVID-19 Saliva Test.

TEST ADMINISTRATION: Staff will instruct you to self-collect your saliva sample by placing the swab tip between your cheek and gum and gently sweeping back and forth along your bottom gum line 10-15 times on each side of your mouth and then under the tongue.  The goal is to saturate the swab with saliva. 

RESULTS: Within 24-48 hpurs of arrival at Quadrant Laboratories, you will receive an email notification that your results are available to view in your profile at:



Test Registration

How to collect your saliva sample

How to create your account profile

Everything under one roof.

Our team does it all. You test with us, our lab processes your samples, your results are reported by us, and we have live people in-house to answer any questions you might have, every step of the way. 

Customer Service:



Years in Business
Team Members
2+ M
COVID tests run
Cups of Coffee

*On September 22, 2020, the Clarifi® COVID-19 Test Kit obtained Emergency User Authorization (EUA) by the Food and Drug Administration (FDA) to be used for the diagnosis of SARS-COV-2. The Clarifi COVID-19 Test Letter of Authorization, along with the authorization Fact Sheet for Healthcare Providers, the authorized Fact Sheet for Patients and authorized labeling are available on the FDA website. 

The Clarifi COVID-19 Test Kit has not been FDA cleared or approved. It has been authorized by the FDA under an emergency use authorization for use by authorized laboratories. Clarifi COVID-19  has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens, and is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostic tests 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.

This test kit is not a direct to consumer test. This test kit is sold only to clinical laboratories in quantity. 

Quadrant Laboratories, a subsidiary of Quadrant Biosciences, is a CLIA certified laboratory that provides individual and pooled COVID testing services ordered by a licensed healthcare provider using the Clarifi COVID Test Kit sold by Quadrant Biosciences.

Note: Testing is limited to qualified laboratories in the United States, certified under the Clinical Laboratory Improvement Amendment of 1988 (CLIA), 42 U.S.C. SS 263A, to perform high complexity testing. 




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