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Both laboratories and methods were certified according to the Clinical Laboratory Improvement Amendments (CLIA 1988) guidelines.
Both laboratories and methods were certified according to guidelines set forth in the Clinical Laboratory Improvement Amendment of 1988.
Both methods were certified (NGSP/Diabetes Control and Complications Trial [DCCT] and International Federation of Clinical Chemistry and Laboratory Medicine [IFCC]).
The laboratory and analytical methods were certified according to guidelines set forth in the Clinical Laboratory Improvement Amendment (U.S. Department of Health and Human Services 1988).
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The laboratory and method were certified according to guidelines set forth in the Clinical Laboratory Improvement Act and Amendment (1988).
This method is certified by the National Glycohemoglobin Standardization Program as traceable to the method used in the DCCT.
This sampling method is certified as producing representative statistics by the Korean Department of Statistics.
The HbA1c method was certified by the National Glycohemoglobin Standardization Program (NGSP) (http://www.ngsp.org/critsumm.asp) and values were International Federation of Clinical Chemistry and Laboratory Medicine (IFCC -aligned.
Moreover, the method was certified annually by an external quality control programme offered by the Society for Advancement of Quality Assurance in Medical Laboratories (INSTAND e.V., Duesseldorf, Germany).
This whole blood automated method is certified and developed to assess eosinophil and neutrophil activity in terms of peroxidase content and cell morphology.
Although the linear dynamic range of the method was certified only down to 100 copies HR-HPV per cell equivalent (Moberg et al, 2003), compared to the five copies described by Gravitt et al (2003), quantification was also possible below that level.
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