Profile: Clinical Controls International offers custom formulations and specialty products, which include whole blood, serum and urine controls, internal and external proficiency performance programs & controls for monitoring drugs-of-abuse and alcohol in the workplace. Our serum ethanol control provides a highly stabilized serum control material that is intended for use in monitoring the accuracy and precision of ethanol determinations. We cater toxicology products like urine ethanol, artificial urine ethanol, ethanol/ammonia, artificial saliva ethanol and whole blood volatiles control. We provide a stabilized serum quality control material intended for use in monitoring the accuracy and precision of ethanol determinations. This serum ethanol control is designed for both enzymatic & GC assays and can be applied to manual & automated methods.
11 Products/Services (Click for related suppliers)
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• Alcohol Control Materials (FDA Code: DKC / 862.3280) A clinical toxicology control material is a device intended to provide an estimation of the precision of a device test system and to detect and monitor systematic deviations from accuracy resulting from reagent or instrument defects. This generic type of device includes various single, and multi-analyte control materials. |
• Assayed and Unassayed Single (Specified) Analyte Controls (FDA Code: JJX / 862.1660) A quality control material (assayed and unassayed) for clinical chemistry is a device intended for medical purposes for use in a test system to estimate test precision and to detect systematic analytical deviations that may arise from reagent or analytical instrument variation. A quality control material (assayed and unassayed) may be used for proficiency testing in interlaboratory surveys. This generic type of device includes controls (assayed and unassayed) for blood gases, electrolytes, enzymes, multianalytes (all kinds), single (specified) analytes, or urinalysis controls. |
• Control Antiserum Antigen Ferritin IGG (FDA Code: DGD / 866.5510) An immunoglobulins A, G, M, D, and E immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the immunoglobulins A, G, M, D, an E (serum antibodies) in serum. Measurement of these immunoglobulins aids in the diagnosis of abnormal protein metabolism and the body's lack of ability to resist infectious agents. |
• Drug Mixture Control Materials (FDA Code: DIF / 862.3280) |
• Drug Specific Control Test (FDA Code: LAS / 862.3280) |
• Drugs Of Abuse Test Kits |
• Enzyme Controls (FDA Code: JJT / 862.1660) |
• Fibrinogen and Fibrin Split Products (FDA Code: DAP / 864.7320) A fibrinogen/fibrin degradation products assay is a device used to detect and measure fibrinogen degradation products and fibrin degradation products (protein fragments produced by the enzymatic action of plasmin on fibrinogen and fibrin) as an aid in detecting the presence and degree of intravascular coagulation and fibrinolysis (the dissolution of the fibrin in a blood clot) and in monitoring therapy for disseminated intravascular coagulation (nonlocalized clotting in the blood vessels). |
• Fibrinogen Control Plasma (FDA Code: GIL / 864.7340) A fibrinogen determination system is a device that consists of the instruments, reagents, standards, and controls used to determine the fibrinogen levels in disseminated intravascular coagulation (nonlocalized clotting within the blood vessels) and primary fibrinolysis (the dissolution of fibrin in a blood clot). |
• General Chemistry Calibrators |
• Multi Analyte Control (FDA Code: JJY / 862.1660) |