Medical dictionary. 2011.
Clinical Laboratory Improvement Amendments — (CLIA) of 1988 are United States federal regulatory standards that apply to all clinical laboratory testing performed on humans in the United States, except clinical trials and basic research.[1] CLIA Program In accord with the CLIA, the CLIA… … Wikipedia
Clinical Laboratory Improvement Act, 1988 — Clinical Laboratory Improvement Act of 1988 (also known as CLIA 88) was presumably passed subsequent to the publication of an article in November 1987 in the Wall Street Journal entitled “Lax Laboratories: The Pap Test Misses Much Cervical Cancer … Wikipedia
Clinical Laboratory Improvement Amendments — Federal legislation, and the personnel and procedures established by it under the aegis of the Health Care Financing Administration (HCFA), for the surveillance and regulation of all clinical laboratory procedures in the U.S.The C. of 1988 (CLIA… … Medical dictionary
Critical Reviews in Clinical Laboratory Sciences — … Wikipedia
Good Clinical Laboratory Practice — (GCLP) ist eine GxP Richtlinie für Laborproben aus Klinischen Studien. Da GCP keine Anforderungen an Prüflabors definiert und GLP für vorklinische Versuche entwickelt wurde und daher nicht auf die spezielle Behandlung von humanen Laborproben aus… … Deutsch Wikipedia
Clinical and Laboratory Standards Institute — (CLSI) is a volunteer driven, membership supported, nonprofit, standards organization. CLSI promotes the development and use of voluntary laboratory consensus standards and guidelines within the health care community. Contents 1 History 2… … Wikipedia
Clinical scientist — This term is frequently used to denote : A biomedical scientist or A clinical laboratory scientist See also Clinical pathologist Clinical biologist Medical laboratory … Wikipedia
Clinical data repository — A Clinical Data Repository (CDR) is a real time database that consolidates data from a variety of clinical sources to present a unified view of a single patient. It is optimized to allow clinicians to retrieve data for a single patient rather… … Wikipedia
Clinical data management — encompasses the entry, verification, validation and quality control of data gathered during the conduct of a clinical trial. Contents 1 Role of the Clinical Data Manager in a Clinical Trial 2 Standard Operating Procedures 3 The Data Management… … Wikipedia
Clinical surveillance — (or Syndromic surveillance) refers to the surveillance of health data about a clinical syndrome that has a significant impact on public health, which is then used to drive decisions about health policy and health education. This is distinct from… … Wikipedia
