clinical laboratory
1Clinical 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… …
2Clinical 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 …
3Clinical 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… …
4clinical laboratory — a laboratory for measurement and examination of materials derived from the human body (e.g., fluids, tissues, cells) for the purpose of providing information on diagnosis, prognosis, prevention, or treatment of disease …
5Critical Reviews in Clinical Laboratory Sciences —   …
6Good 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… …
7Clinical 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… …
8Clinical scientist — This term is frequently used to denote : A biomedical scientist or A clinical laboratory scientist See also Clinical pathologist Clinical biologist Medical laboratory …
9Clinical 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… …
10Clinical 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… …
