| Literature DB >> 10667685 |
Abstract
Many strategies have been promulgated for the setting of quality specifications in laboratory medicine. Based on the analysis of the effect of error on clinical decision making, general quality specifications for precision, bias, the allowable difference between two analytical methods, drugs, fixed limits for use in external quality assessment and reference methods seem best derived from components of biological variation.Mesh:
Year: 1999 PMID: 10667685 DOI: 10.1080/00365519950185210
Source DB: PubMed Journal: Scand J Clin Lab Invest ISSN: 0036-5513 Impact factor: 1.713