
AFP, CEA and CA series assigned national values to support IVD performance evaluation and EQA.
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Patented stabilisation technology extends open-vial stability beyond the typical two-day benchmark.
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Recognition of our research and product capabilities supports continued investment in independent quality-control development.
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Broader concentration ranges support reagent performance evaluation and registration testing.
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Custom serum-panel preparation and quality controls for reagent manufacturers and laboratories.
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The quality-management system continues to support product consistency.
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Expanded thyroid and sex-hormone analytes strengthen the reference-material portfolio.
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Improved capacity and lot consistency support supply at scale.
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The new website improves product presentation, technical support and traceability search.
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Independent, traceable quality controls are becoming a common language for performance comparison.
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External quality assessment for infectious-disease immunoassays across regional laboratories.
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Experts discuss performance-verification practice under ISO 15189.
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A review of metrological traceability and uncertainty requirements in registration submissions.
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The value of serum panels in sensitivity, specificity and agreement evaluation.
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Using mutant serum panels to assess missed-detection risk and reagent coverage.
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Value assignment and evaluation principles based on JJF 1059 and ISO Guide 35.
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Result interpretation and quality-improvement recommendations for regional laboratories.
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Methods for assessing reference-material commutability across testing systems.
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