CLIA Waived Documents

The Clinical Laboratory Improvement Amendments of 1988 (CLIA) establishes quality standards for laboratory testing to ensure the accuracy, reliability, and timeliness of patient test results. The Food and Drug Administration (FDA) has approved several rapid HIV tests including the one you received during your visit. Approved rapid tests may be used in clinical and non-clinical testing sites, including community and outreach settings. As required by the FDA,  below you will find more information about the services you were provided. If you have any questions, please email us at We hope that you visit us soon!

HIV OraQuick Customer Letter

Syphilis_Trinity Biotech

HIV_Insti Use

HIV_Alere Subject Notice

HCV_OraQuick Customer Letter

HIV_Alere Subject Notice