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About ARUP Laboratories We are a CAP-, ISO 15189-, and CLIA-certified diagnostic laboratory with more than 40 years of experience supporting hospital and health system clients with unparalleled quality and service Beyond offering quality testing, our goals include innovating, improving continuously, changing the future of laboratory medicine, and supporting our clients’ success in patient care while helping
Testing Specialties - ARUP Laboratories Testing Specialties This page highlights our testing specialties, test updates, testing resources, compliance statements, and experts
ARUP Laboratories | National Reference Laboratory ARUP provides reference laboratory testing for hospitals and health centers, serving the diagnostic needs of patients We also consult on lab management, utilization, and operations
Compliance - ARUP Laboratories ARUP Compliance Policy ARUP abides by regulations pertaining to the appropriate language for labeling non-FDA approved test methods offered by ARUP
Education - ARUP Laboratories We apply our academic expertise to improve patient care by providing over 145,000 continuing education credits annually for clients, physicians, and laboratory professionals at no cost, through our online CME, P A C E ®, and Florida continuing education courses
LOINC Codes - ARUP Laboratories Logical Observation Identifier Names and Codes (LOINC), the international standard for coding laboratory results, provides universal code names and identifiers for laboratory tests and other medical terminology that can be used in medical health records LOINC facilitates interoperability and communication within healthcare networks by providing a standard vocabulary for the universal
ARUP Laboratory Test Directory | ARUP Laboratories ARUP’s Laboratory Test Directory is a publicly accessible site that gives complete and up-to-date information about the tests that we perform here at ARUP It offers ordering recommendations, details acceptable specimens including volume, and transportation and storage instructions There is also access to ARUP Consult™ disease topics, interpretive information, and reference ranges For
The FDAs Final Rule on Laboratory-Developed Tests: FAQs What does the FDA’s final rule on LDTs change? The rule makes it explicit that in vitro diagnostics (IVDs) that are manufactured by clinical laboratories—i e , laboratory-developed tests (LDTs)—are considered devices under the Federal Food, Drug, and Cosmetic Act (FDCA) IVDs are tests performed on samples such as blood or tissue that have been taken from the human body LDTs are
Licensure Accreditations - ARUP Laboratories ARUP participates in the College of American Pathologists (CAP) Laboratory Accreditation Program and has CLIA (Clinical Laboratory Improvement Amendments) certification through CMS (Centers of Medicare and Medicaid Services) ARUP also holds current licensure or permits required by state or local regulations Note to clients: ARUP Laboratories' accreditation by CAP complies with CAP Laboratory