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For use with the INDICAID® (Professional) COVID-19 Rapid Antigen Test
USA SALES ONLY
A VALID CLIA NUMBER IS REQUIRED FOR PURCHASE.
ENTER CLIA NUMBER IN THE SHOPPING CART AT THE TIME OF PURCHASE.
Each box contains 5+/5- Control vials.
*PLEASE ORDER SEPARATELY AS SPECIAL, COLD SHIPPING IS REQUIRED
**ONLINE PURCHASES ARE LIMITED TO 100 BOXES CONTAINING 500+/500- CONTROLS.
***FOR ORDERS OVER 100 BOXES, PLEASE CONTACT OUR SALES PROFESSIONALS.
The INDICAID® COVID-19 Antigen Quality Controls are intended for quality control testing performed on the INDICAID® COVID-19 Rapid Antigen Test. The Quality Controls provide users with assurance that the device is performing within specification.
The INDICAID® COVID-19 Antigen Quality Controls are external liquid quality controls. The controls are specifically formulated and manufactured to ensure that the test’s reagents and materials are working and that the test procedure is correctly performed. The Quality Controls consist of positive and negative control samples that should be run once with every new lot, shipment, using the test procedure provided.
It is the responsibility of each laboratory or healthcare operation using the INDICAID® COVID-19 Rapid Antigen Test to establish an adequate quality assurance program to ensure the performance of the test kit under its specific locations and conditions of use. Quality control requirements should be followed in conformance with local, state, and federal regulations or accreditation requirements and the user laboratory’s standard quality control procedures.
To review and download INDICAID® documentation, including Instructions For Use (IFU), Safety Data Sheet, FDA EUA, Fact Sheet for Healthcare Providers, Quick Reference Guide, FAQs, and more, please visit our website 'Download' section.
NOTE: Expiration Date: If you receive a box that has an expiration date that has passed, please do not be concerned. The FDA has granted an extended expiration life by 6 months from the expiration date printed on the back of the box for these tests. Read the FDA EUA Expiration Update document.
The Clinical Laboratory Improvement Amendments of 1988 (CLIA) regulations include federal standards applicable to all U.S. facilities or sites that test human specimens for health assessment or to diagnose, prevent, or treat disease. CDC, in partnership with CMS and FDA, supports the CLIA program and clinical laboratory quality. Learn more about CLIA.
INDICAID® COVID-19 Rapid Antigen Test Device
INDICAID® COVID-19 Rapid Antigen Test Buffer Solution Vial
INDICAID® COVID-19 Rapid Antigen Test Individually Wrapped Swab
If the external controls do not produce the expected results, do not use the test for patient testing or report patient results. Please contact PHASE Scientific Technical Support during normal business hours before using the test with patient specimens.
*Cold Shipping Is Required. We only ship the product via FED-EX Overnight Monday-Thursday to guarantee delivery on business days only.