Clinical Pathology

  • Multichem ID-SeroNeg Infectious Disease (ID) Quality Controls samples
    Negative multi-marker QC Multichem Infectious Disease (ID) Quality Controls (QC) samples, have been specifically optimised and validated to match assays commonly used for infectious diseases testing. Multichem ID-SeroNeg provides a negative control for the analytes listed below. Scroll down to view the product benefits and analyte list. Multichem ID SeroNeg provides a third party, unassayed, negative control for commonly tested assays for anti-HIV, anti-HCV, anti HTLV, anti-HBc, anti-Treponema, HBsAg and HIVp24
  • Neonatal Bilirubin QC
    Third party, single elevated level, liquid stable quality control material to monitor the precision of laboratory testing procedures for Bilirubin and Theophylline Assays. Multichem NB (Neonatal Bilirubin) Control, from Technopath Manufacturing Ltd, is intended for use as a third party, single level, liquid stable quality control material to monitor the precision of laboratory testing procedures for Bilirubin and Theophylline Assays. An important patient population is Neonates, where a requirement has been identified for testing conditions associated with Neonatal hyperbilirubinemia. The product also contains Theophylline, a therapeutic drug that is given to Neonates to improve lung capacity and where it would be required to monitor for toxicity risk. Caffeine is a listed analyte that is added gravimetrically, and this has a clinical function as the primary treatment of the breathing disorders apnea of prematurity. Another important population is with any patient that has liver failure. It is important if the laboratory tests hyperbilirubinemia patient samples that they analyze QC regularly to monitor this range to ensure accuracy and precision at these elevated levels. The requirement for a high concentration of Bilirubin presents a conflict for consolidation of multi-analytes. This means that not only is a separate paediatric control required, but a control matrix that is treated with antioxidants to inhibit the oxidation of Bilirubin. The application of the most appropriate measures to reduce the effect of oxidation on the high levels of Bilirubin in the Control have been researched to ensure that open vial and closed stability is maintained. Multichem NB Control is designed as a single level, liquid stable frozen product. The product will typically be run as a supplementary high level control, in conjunction with at least one of the Multichem Serum Control levels, (S or S Plus) to provide a minimum of 2 levels of control to allow assay system performance monitoring within the analytical ranges. It will be run after reagent calibration and at a frequency dictated by laboratory QC procedures and reagent / instrument manufacturer instructions. The product should be treated the same as patient specimens and run in accordance with the instructions accompanying the instrument, kit or reagent being used. The control is to be stored at -20°C to –80°C and thawed as per IFU prior to use. The product is to be stored at 2 to 8°C between use.
  • Multichem P (P for protein), from Technopath Manufacturing Ltd, is specifically designed as a supplementary QC product for immunoproteins to be used in conjunction with the Multichem clinical chemistry QC. This product offers elevated concentrations for immunoprotein. Users can use this in conjunction with 1, 2 or 3 levels of Multichem S Plus or Multichem S, each of which already include multiple concentrations for immunoproteins. The full list of products available are shown below. Multichem P Supplementary Immunoprotein Control is intended for use as a third party, single level, liquid stable immunoprotein quality control material to monitor the precision of laboratory testing procedures for Immunoprotein Assays. Target values are provided for 39 analytes, including immunoglobulins, complement proteins, inflammatory proteins as well as carrier and storage proteins. The product will typically be run as a supplementary high level control, in conjunction with at least one of the Multichem Serum Control levels, (S or S Plus) to provide a minimum of 2 levels of control to allow assay system performance monitoring within the analytical ranges. It will be run after reagent calibration and at a frequency dictated by laboratory QC procedures and reagent / instrument manufacturer instructions. The product should be treated the same as patient specimens and run in accordance with the instructions accompanying the instrument, kit or reagent being used. The control is to be stored at -20°C to –80°C and thawed as per IFU prior to use. The product is to be stored at 2 to 8°C between use.
  • Multichem S Plus Serum Chemistry & Immunology QC
    Multichem S Plus Control, from Technopath Manufacturing Ltd,  is intended for use as a third party, multi-constituent quality control material to monitor the precision of laboratory testing procedures for Chemistry Assays. It incorporates serum chemistry, immunology, lipid, TDM, enzymes and esoterics. Multichem S Plus contains 105 analytes including the addition of C-Reactive Protein and Rheumatoid Factor at clinically relevant concentrations. Chemistry, Esoterics, Immunoproteins, Enzymes, Lipids, and Therapeutic Drugs are also included. When combined with Multichem P the solution offers an extensive spread of immunoprotein concentrations. Multichem S is also available, please note that Multichem S contains all the same analytes apart from C-Reactive Protein and Rhematoid Factor. Multichem S Plus is designed as a tri-level, liquid stable frozen product. This product will typically be run after reagent calibration and at a frequency dictated by laboratory QC procedures and reagent / instrument manufacturer instructions. The product should be treated the same as patient specimens and run in accordance with the instructions accompanying the instrument, kit or reagent being used. The control should be stored at -20°C to –80°C and thawed as per IFU prior to use. The product should be stored at 2 to 8°C between use.
  • Multichem U Control, from Technopath Manufacturing Ltd, is intended for use as a third party, bi- level, liquid stable, multi-analyte control designed for use in the routine monitoring of precision of laboratory testing procedures. Target values are provided for 13 analytes including kidney function parameters, pituitary/adrenal metabolites, hCG and urinary proteins. Multichem U Control is designed as a bi-level liquid stable product. The product will typically be run after reagent calibration and at a frequency dictated by laboratory QC procedures and reagent / instrument manufacturer instructions. The product should be treated the same as patient specimens and run in accordance with the instructions accompanying the instrument, kit or reagent being used. The control is to be stored at 2°C to 8°C and mixed as per IFU prior to use. The control is to be stored at 2 to 8°C between use.
  • Multichem WBT Control, from Technopath Manufacturing Ltd,  is intended for use as a third-party, tri- level, liquid stable quality control material to monitor the precision of laboratory testing procedures for Cyclosporine, Tacrolimus and Sirolimus Assays. Multichem WBT Control is designed as a tri-level, liquid stable frozen product. The product will typically be run after reagent calibration and at a frequency dictated by laboratory QC procedures and reagent / instrument manufacturer instructions. The product should be treated the same as patient specimens and run in accordance with the instructions accompanying the instrument, kit or reagent being used. The control is to be stored at -20°C to –80°C and thawed as per IFU prior to use. The product is to be stored at 2 to 8°C between use.
  • Liquid Handling
    Ensure pipettes are performing properly and operator skills are standardised Manage your pipette calibration program and assess operator competency. Used in combination with the Artel PCS, the PCS Software ensures your pipettes and their operators are working together to generate accurate and reproducible results. The PCS Software provides scheduling for pipette calibrations and interim performance verifications; complete documentation and pipette inventory management, even for pipettes calibrated outside of PCS Software – and it’s ideal for standardising pipetting technique and assessing operator competency.  
  • CE Marked Routine Coagulation Controls from Biomedica Diagnostics are intended to be used as unassayed controls for monitoring the performance of routine coagulation assays on analysers in a clinical setting. The controls are to be tested in the same manner as freshly drawn citrated patient plasma. The controls are available within the normal and abnormal ranges and suitable for use in four (4) parameters.
  • Baebies Logo SEEKER Newborn Screening Platform
    Newborn screening platform powered by digital microfluidics SEEKER® is a newborn screening laboratory solution that performs multiple assays at the same time using just one punch from a newborn dried blood spot specimen.  SEEKER® is used to test thousands of babies each day around the world. Lysosomal Storage Disorders SEEKER® is the first FDA-authorised and CE-marked newborn screening platform for lysosomal storage disorders. SEEKER® quantitatively measures the activity of lysosomal enzymes from newborn dried blood spot specimens. Reduced activity of these enzymes may be indicative of: MPS I • Pompe • Gaucher • Fabry
  • Fortress Diagnostics Fortress Diagnostics Serum Indices
    Your perfect tool to aid in the monitoring of instrument detection of Haemolysis, Icterus and Lipaemia in specimens. Fortress Serum Indices Quality Control are designed to monitor the ability of an instrument to accurately measure HIL in specimens. This is done through the manufacture of control material which mimics specimens that would be considered normal, haemolytic, icteric, and lipaemic using human based products. Ensure accurate monitoring of patient samples for Serum Indices by running this QC daily.
  • Special Coagulation Control from Biomedica Diagnostics
    CE Marked Special Coagulation Controls from Biomedica Diagnostics are intended to be used as unassayed controls for monitoring the performance of special and routine coagulation assays on analyzers in a clinical setting. The controls are to be tested in the same manner as freshly drawn citrated patient plasma. The controls are available within the normal and abnormal ranges and suitable for use in eighteen (18) parameters.
  • LGC Maine Standards Logo VALIDATE® ACTH
    ACTH Chemistry Linearity Verification and Calibration Kits Adrenocorticotropic Hormone analyte for your Roche cobas® clinical analyser.
    • CE Marked
    • Adrenocorticotropic Hormone Analyte Available
    • Human Plasma Matrix
    • Liquid, Ready-to-Use
    Analyte Summary by available Product ACTH: ACTH
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