Located in Hudson, Ohio, DNA Analytical Services LLC is dedicated to bringing Personalized Medicine to the greatest number of people through Medical DNA Testing
We offer the most comprehensive FDA approved DNA Hereditary cancer analysis report and state-of-the-art DNA drug interaction reports available in the country today through churches, synagogues, non-profit organizations, and corporations – to those qualified with commercial insurance, Medicare, and Tricare.
Our Medical Laboratories specialize in genetic testing and we have performed thousands of tests to the highest standards for doctors all over the country.
Each year we are recognized as having the Clinical Standards and Quality of the Clinical Laboratory Improvement Amendment as regulated by the Center for Medicare and Medicaid Services. We are …
The Food & Drug Administration (FDA)
The Center for Disease Control and Prevention (CDC)
The Center for Medicare and Medicaid Services (CMS)
Accredited by the College of American Pathologists (CAP)
State licensed in New Jersey and Georgia
Compliant with HIPPA privacy guidelines & regulations
Diagnostic testing helps health care providers screen for or monitor specific diseases or conditions. It also helps assess patient health to make clinical decisions for patient care. The Clinical Laboratory Improvement Amendments (CLIA) regulate laboratory testing and require clinical laboratories to be certificated by their state as well as the Center for Medicare and Medicaid Services (CMS) before they can accept human samples for diagnostic testing. Laboratories can obtain multiple types of CLIA certificates, based on the kinds of diagnostic tests they conduct.
Three federal agencies are responsible for CLIA: The Food and Drug Administration (FDA), Center for Medicaid Services (CMS) and the Center for Disease Control (CDC). Each agency has a unique role in assuring quality laboratory testing.
FDA – Categorizes tests based on complexity AND Develops rules/guidance for CLIA complexity categoriza
CMS – Conducts inspections and enforces regulatory compliance and Monitors laboratory performance on Proficiency Testing (PT) and approves PT programs
CDC – Provides analysis, research, and technical assistance … Develops technical standards and laboratory practice guidelines, including standards and guidelines for cytology … Conducts laboratory quality improvement studies … Monitors proficiency testing practices