Attention: Clinical Laboratory Professionals
Please share the following with:
Medical Director, Laboratory Services
The Centers for Medicare & Medicaid Services (CMS) has issued a statement in response to recent confusion regarding quality control for tests with FDA emergency use authorization (EUA). See below for the statement from CMS:
“The manufacturer’s instructions for all tests that have authorization for use as EUA must be followed, to include quality control (QC). Surveyors will ensure that the laboratory is following the EUA Instructions for Use (IFU) as well as its own established policies, specifically its QC procedures. QC for EUAs must be followed, and no deviations to the QC requirements in the EUA are permitted; Individualized Quality Control Plan (IQCP) is not applicable to EUAs. Please note: The laboratory director may determine, based on risk assessment, that additional QC needs to be implemented above what is required in the EUA IFU. Please also note: States and Accreditation Organizations (AOs) may have more stringent requirements.”
In addition, on Tuesday, November 10, CMS updated the Clinical Laboratory Improvement Amendments (CLIA) frequently asked questions (FAQ) document to provide further clarification on IQCP and added several new FAQs regarding CLIA certificates. Click here to view the document.
- Individualized Quality Control Plan (IQCP)
- Clinical Laboratory Improvement Amendments (CLIA)
- Interim Guidance for Rapid Antigen Testing for SARS-CoV-2
- Information for Laboratories about COVID-19
- Frequently Asked Questions about COVID-19 for Laboratories
- CDC Laboratory Outreach Communication System (LOCS)
- Clinical Laboratory COVID-19 Response Calls
- Register for CDC Health Alert Network (HAN) notifications, including updates about COVID-19. Enter your email address, search for HAN, and sign up.
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