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Clinical Chemistry|September 23, 1997
Application of the Department of Health and Human Services proposed waived status requirements for in vitro diagnostic testing devices: case studyS S Ehrmeyer, R H LaessigClinical Chemistry|January 1, 1985
Alternative statistical approach to evaluating interlaboratory performanceS S Ehrmeyer, R H LaessigClinical Chemistry|June 1, 1987
Ability of the 1(2)s rule to detect substandard performance in interlaboratory proficiency testingS S Ehrmeyer, R H LaessigClinica Chimica Acta; International Journal of Clinical Chemistry|May 23, 2001
Electronic "Quality Control" (EQC): is it just for unit use devices?S S Ehrmeyer, R H LaessigClinical Chemistry|September 1, 1988
Use of computer modeling to predict the magnitude of intralaboratory error tolerated by proposed CDC interlaboratory proficiency testing performance criteriaR H Laessig, S S EhrmeyerClinical Chemistry|August 1, 1985
Adequacy of interlaboratory precision criteria in measuring intralaboratory performanceS S Ehrmeyer, R H LaessigClinical Chemistry|June 1, 1987
Interlaboratory proficiency-testing programs: a computer model to assess their capability to correctly characterize intralaboratory performanceS S Ehrmeyer, R H LaessigAmerican Journal of Clinical Pathology|January 1, 1988
The relationship of intralaboratory bias and imprecision on laboratories' ability to meet medical usefulness limitsS S Ehrmeyer, R H LaessigClinical Chemistry|October 1, 1987
An assessment of the use of fixed limits to characterize intralaboratory performance by proficiency testingS S Ehrmeyer, R H LaessigPageof 5