The kit is designed for daily intralaboratory control of correctness and reproducibility of the reagent-analyser system in determining the following haemostasis parameters in normal and pathological areas:prothrombin according to Quick in % of normal; prothrombin index, %; prothrombin ratio (International Normalised Ratio, INR);thrombin time, sec;activated partial thromboplastin time (APTT), sec;fibrinogen content according to Clauss, g/l;antithrombin III (ATIII) activity, %;total fibrinolysis system (XIIa-dependent fibrinolysis), min. Set composition: Human blood plasma with haemostasis parameters within normal limits, lyophilically dried (1 ml/fl.) - 3 vials.Human blood plasma with artificially reduced parameters of haemostasis, lyophilically dried (1 ml/fl.) - 3 vials.
Number of determinations in 1 set: 120.
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