the application must be delivered to the local agency for the state in which the laboratory facility is located. (A current list of state agencies can be found on theCMS website.) Some survey agencies have state-specific requirements, so it’s always prudent to contact the ...
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If the tests are performed for these purposes, the organization doing so is considered under CLIA to be a laboratory and must register with the CLIA program. In these instances, the advantage of using a “CLIA Waived” test is that it “waives” you from having to comply with a long ...
“We are very pleased to receive the Certificate of Compliance for the Melbourne laboratory from the CMS,” said Dr. Paul MacLeman, Genetic Technologies’ Chief Executive Officer. “The certificate is an essential component of our business strategy, and we are...
This software package is designed to assist the clinical laboratory in meeting minimum regulatory requirements for method evaluation and validation. System requirements are modest (PC with a 486 CPU, 8 MB RAM, and 10 MB hard drive space); the operating systems supported are Windows 95, 98, or...
has been chosen as the location for the headquarters of Immunovia Inc, a wholly owned subsidiary of Immunovia AB, and that the facility agreements have been finalized. This new Immunovia site is designed to accommodate a CLIA accredited reference laboratory for theEastern USAas...