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TID : 74737673 | Dept Tender Number :| Tender Type :Buy
Supply of Biochemistry Reagents and Kits - Glucose– Liquid with standard, linearity 600 mg/dl & above (Glucose oxidase/Hexokinase), Cholesterol – with standard, linearity 1000 mg/dl (Cholesterol oxidase), Urea – Kinetic with standard, linearity 500 mg/dl (Urease Kinetic), Creatinine – with standard, linearity 20 mg/dl & above (Enzymatic/Jaffe modified), Phosphorus – Liquid stable ready to use with standard, linearity 15 mg/ml & above (U.V. end point using ammonium molybdate), Uric Acid – with standard liquid stable standard, linearity 20 mg/dl & above (Uricase peroxidase with no ascorbate oxidize), Triglyceride – with standard, linearity 1000 mg/dl & above (GPO-PAD), Calcium – Liquid stable with standard linearity 20 mg/dl& above (Arsenzoe III), Phospholipid – with standard linearity 500 mg/dl & above {CHO (Choline oxidize) – POD(presence of peroxide enzymatic – colorimetric)}, SGOT – Kinetic, linearity 500 U/l& above (IFCC without pyrdoxal phosphate method two reagent kit) (Liquid stable reagent), SGPT – Kinetic, linearity 500 U/l & above (IFCC without pyrdoxal phosphate method two reagent kit) (Liquid stable reagent), LDH – Liquid stable, linearity 1500 u/l & above (P ?L method) IFCC, CPK-NAC – Liquid stable, linearity 1500 U/l & above (Creatinine kinase kinetic IFCC method)), CPK MB –liquid stable, linearity 2000 U/l & above, kinetic (NADH Kinetic) with control & Calibrator, Amylase – Liquid stable, linearity 2000 U/l and above (Kinetic using CN PG3), Lipase – Kinetic, linearity 700 u/l, with standard and controls (Enzymatic colorimetric ), Alkaline Phosphatase – Kinetic, linearity 1000 u/l (IFCC or AACC optimized method using AMP buffer), Total Protein – Linearity 15 gm/dl & above(Biuret) , Albumin – Linearity 7 gm/dl & above (Bromocresol green) , Iron + TIBC – Liquid stable, linearity up to 600 mg/dl suitable for fully auto Analyzer Ferrozine method) , Acid Phosphates – Kinetic, linearity 80 u/l & above (NaphthyI Phosphate Kinetic with pentaanedise activation), Bilirubin – Biochromatic kit suitable for Auto analyzer, linearity 20 mg/dl & above preferably single reagent for total and direct bilirubin (Diazo with sulphanilic acid), "LDL Cholesterol – (Direct) suitable for , Auto Analyzer, linearity 1000 mg/dl & above with calibrator & control. Calibrator should be traceable to internationally accepted norms., ", Gamma GT – Liquid stable, linearity 250 u/l & above (IFCC CY – glutamyl 3 – Carboxy 4 Nitroanilide), "Quality Control (Normal) Human sera based, 1. Assigned values should be available for major automated analyzers, making this control a highly efficient solution for laboratories that focus on routine tests., 2. Quality control should be aqueous, clear matrix, 3. Quality control should have 3 year shelf life at 2-8°C , 4. Quality control can be stored for up to 12 month at 20-25°C , 5. Should have open vial stability at least 25 to 30 days., 6. Quality control should be USFDA approved, 7. Quality control provider should offer peer group reports as and when required., 8. Company should have offer of QC Data management solutions & connectivity to support controls., 9. Company should offer inter laboratory program, 10. Company should offer individual laboratory comparison report with Bias and Histogram Report, 11. Company should offer affiliated laboratory comparison report., 12. Company should offer monthly evaluation report, 13. Traceable certificate to be enclosed, ", "Quality Control (Abnormal) Human sere based, , 1. Assigned values should be available for major automated analyzers, making this control a highly efficient solution for laboratories that focus on routine tests., 2. Quality control should be aqueous, clear matrix, 3. Quality control should have 3 year shelf life at 2-8°C , 4. Quality control can be stored for up to 12 month at 20-25°C , 5. Should have open vial stability at least 25 to 30 days., 6. Quality control should be USFDA approved, 7. Quality control provider should offer peer group reports as and when required., 8. Company should have offer of QC Data management solutions & connectivity to support controls., 9. Company should offer inter laboratory program, 10. Company should offer individual laboratory comparison report with Bias and Histogram Report, 11. Company should offer affiliated laboratory comparison report., 12. Company should offer monthly evaluation report, 13. Traceable certificate to be enclosed, ", "HbA1c – Kit suitable for Auto Analyzer with calibrator, 1.Should be NGSP and IFCC approved., 2. Quality control should be third party., 3. Turbidometric inhibition immunoassay or Enzymatic, ", "Multi-analyte Calibrator for calibrating biochemical parameters should be traceable to internationally accepted standards/ norms., 1. Should be human sera based., 2. Should have long stability, 3. Should have maximum number of biochemical parameters., ", Total Lipids – with standard linearity up to 1500 mg/dl & above, ready to use for Auto Analyzer , CSF Protein – Linearity up to 250 mg/dl with standard and calibrator. Minimum of 2 vials per kit calibrator should be provided with each kit. (2 x 3 ml), "CSF Protein quality control-5ml, 1. Human based material, 2. True third party control providing unbiased performance assessment, 3. Assayed target values available, 4. Shelf life of 2 years from the date of manufacture, 5. Open vial stability of 30 days for all analytes when stored at 2°C to 8°C, ", HDL Cholesterol – (Direct) clearance two reagent method suitable for auto analyzer linearity up to 180 mg/dl with calibrator and control. Calibrator should be traceable to internationally accepted norms. Control and calibrator volume approx. 3 ml per kit., "Blood Gas, Quality control material should be designed to meet the expanded test menus of today’s blood gas analyzers. :- , 1. Quality control should include Ph, Blood Gas, Electrolytes and Metabolites., 2. Quality control should be aqueous, clear matrix, 3. Quality control can be stored for up to 12 months at 20-25°C, 4. Quality control should be USFDA approved, 5. Quality control provider should offer peer group reports as and when required., 6. Analytes:, 1) Calcium(Ionized), 2) Chloride, 3) Glucose, 4) Lactate(Lactic Acid), 5) pCO², 6) Ph, 7) pO², 8) Potassium, 9) Sodium, 10) TotalCO²", "Quality Control Tri – Level – For routine monitoring of both accuracy and precision with assayed instrument specific target values. Including fertility, steroid-thyroid hormones, tumor marker, vitamins etc., Minimum Parameters, Free T3, Free T4, TSH Anti TPO (Anti oxidaze ), FSH, LH, , Prolactin, Beta HCG, Testosterone, Cortisol, Growth Hormone, (HGH) , PTH, Insulin, Ferrtin, Vitamin B12, , Folate, CEA , Alpha Feto Protein (AFP), , PSA , Total IgE, Vitamin D , Anti CCP, CA -125 , 1. Lyophilized human origin serum, 2.Reconstituted stability of at 2°C to 8°C, at least 25 days at 20°C, 3. Assigned values should be available for major automated analyzers, making this control a highly efficient solution for laboratories that focus on routine tests., 4. Quality control should be USFDA approved, Quality control provider should offer peer group reports as and when required., ", "Serum Magnesium – 1) Method – Calmagide Method , 2) Linearity 5 mg/dl& above with control & Calibrator 3) Liquid stable suitable for fully automated analyzer. at Jaipur,Rajasthan,India