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  2. Clinical Laboratory Improvement Amendments - Wikipedia

    en.wikipedia.org/wiki/Clinical_Laboratory...

    A CLIA Certificate of Compliance (CoC). Per CLIA, each specific laboratory system, assay, examination is graded for level of complexity by assigning scores of 1, 2, or 3 for each of the following seven criteria.

  3. College of American Pathologists - Wikipedia

    en.wikipedia.org/wiki/College_of_American...

    The COM checklist also describes the requirements for analytical validation/verification of the method performance specifications (i.e. accuracy, precision, reportable range) that laboratories must perform for each test, method, or instrument system before use in patient testing. [10]

  4. Validation and verification (medical devices) - Wikipedia

    en.wikipedia.org/wiki/Validation_and...

    Standards for validation and verification of medical laboratories are outlined in the international standard ISO 15189, in addition to national and regional regulations. [1] As per United States federal regulations, the following analytical tests need to be done by a medical laboratory that introduces a new testing device:

  5. Individualized Quality Control Plan - Wikipedia

    en.wikipedia.org/wiki/Individualized_Quality...

    The Individualized Quality Control Plan (IQCP) is a quality management system under the US Clinical Laboratory Improvement Amendments (CLIA) federal regulatory standards. It is designed to enable regulated medical laboratories to manage the frequency of their quality control .

  6. ISO 15189 - Wikipedia

    en.wikipedia.org/wiki/ISO_15189

    ISO 15189 Medical laboratories — Requirements for quality and competence is an international standard that specifies the quality management system requirements particular to medical laboratories. The standard was developed by the International Organisation for Standardization 's Technical Committee 212 (ISO/TC 212).

  7. Laboratory quality control - Wikipedia

    en.wikipedia.org/wiki/Laboratory_quality_control

    Validation or verification is generally needed when a health facility acquires a new device to perform medical tests. The main difference between the two is that validation is focused on ensuring that the device meets the needs and requirements of its intended users and the intended use environment, whereas verification is focused on ensuring ...

  8. What NFL games are tomorrow? Full schedule, how to watch ...

    www.aol.com/nfl-games-tomorrow-full-schedule...

    Sunday's Week 12 NFL games includes several intriguing matchups that will dictate the direction the NFC West race heads as the playoffs near.

  9. Clinical and Laboratory Standards Institute - Wikipedia

    en.wikipedia.org/wiki/Clinical_and_Laboratory...

    CLSI provides direct assistance in Sub-Saharan Africa to combat HIV/AIDS and other infectious diseases. With grants from the US-based PEPFAR (President's Emergency Plan for AIDS Relief) program administered by a cooperative agreement from the Centers for Disease Control and Prevention (CDC) and the National Institute of Allergy and Infectious Diseases (NIAID), CLSI has been actively involved ...