ge healthcare

Benchtop-sized image cytometer

The launch of the Cytell Image Cytometer, a benchtop-sized image cytometer for rapid cell characterisation, introduces researchers to a new, simpler, faster and more productive way to conduct their cell analysis. The new system enables researchers to capture detailed data about their cells quickly while using minimal sample volumes. Data can be acquired for up to eight samples at a time and results are delivered through an intuitive graphical interface in less than two-and-a-half minutes. The system simplifies researchers’ working practices and increases productivity by removing the need to use specialised cell analysis instruments. Large cell analysis instruments are often in a shared facility, which can be difficult to access at the right time, and are time-consuming to use.
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seracare

HPV qualification panel

A new HPV genotype qualification panel expands the Sera- Care Women’s Health portfolio in response to the rapidly rising demand for products designed to meet the requirements for HPV assay qualification. The panel is derived from cultured human cells containing fulllength HPV DNA and includes the HPV 16 and HPV 18 genomes, which together account for an estimated 70 percent of all cases of the virus. The panel is designed to support assay qualification and testing by challenging every step in the process, from extraction through detection. The panel is designed for use with HPV test kits from Roche Molecular Diagnostics, Qiagen/digene and Hologic. In addition to supporting the vital process of assay verification, the panel can also be used for method comparison, reproducibility and lot-to-lot variability studies.
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Liquid tumour marker control

Covering a total of 15 commonly tested and esoteric cancer antigens and tumour markers, the Acusera multi-analyte liquid tumour marker control is ready to use. The material is highly convenient and easy for laboratory staff. The addition of assayed target values enables laboratories to effectively monitor measurements with both accuracy and precision. The liquid stable nature not only eliminates the need for reconstitution but reduces the amount of human handling necessary and allows the material to be shipped and stored conveniently at 2-8oC. The serum is 100% human in origin providing a matrix similar to the patient sample but also reducing antibody interference and the possibility of control values shifting after changing reagent batch. Three distinct and clinically significant levels of control are available with analytes present at desirable levels. The convenient 6 x 3mL pack size and refrigerated open vial stability of 30 days for all analytes helps to increase laboratory efficiency while keeping waste and costs to a minimum. As a true third party control laboratories can use it to independently assess the performance of their tumour marker testing. Fully assayed, instrument specific target values are generated via a number of external laboratories and are provided for many common clinical chemistry and immunoassay systems. The control is compatible for use with Acusera 24.7, a web based inter-laboratory data management programme. With 24-7 users benefit from the company’s extensive range of data management tools and gain access to peer group data from thousands of laboratories worldwide. The programme uniquely updates peer group data every 24 hours giving laboratories access to the most up to date information available.
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noema

Web-based clinical lab computerisation system

A new middleware for clinical chemistry, microbiology and molecular biology labs is available. Utilising a rule-based engine to deliver all-round control over laboratory workflow and sample processing, HALIA’s powerful functionality significantly improves laboratory efficiency, compliance and quality control. The middleware interface provides a complete web-based lab computerisation system, allowing central management and connection of all analysers through a single interface on any workstation. The user-configurable rule-based engine enables autoverification, sample routing and real-time clinical data capture and management for greater quality control. By supporting open automation systems and addressing issues such as regulatory compliance, workforce reductions and enhanced quality control, this middleware effectively meets the challenges facing lab managers. Responding to the increase in Point of Care Testing, a POCT Data Manager function is offered. This gives lab managers a real-time overview of all the data relating to multiple blood gas analysers or other devices, including instrument maintenance schedules and QC alerts. Detailed real-time data on total turnaround time (TAT) – a key performance indicator in large laboratories striving to increase throughput – is also provided. If a LIS/LIMS system goes down, the backup module allows manual input of sample information. Manual samples are then matched to LIS/LIMS data once the connection is restored.
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thermo

Durable universal polypropylene containers

Ideal for protecting samples in all types of laboratories, Sterilin Quick Start 30mL polypropylene universal containers are leakproof, resistant to temperature and chemicals and easier to use. The containers are manufactured from clear polypropylene, which has greater temperature and chemical resistance than other materials such as polystyrene. This meets the needs of a wider range of laboratory applications, from healthcare to life science research. The new containers have a Quick Start cap with a threestart thread, reducing the number of turns to open and close it. In an independent evaluation against similar products, the containers’ new multi-seal design provided unrivalled leak-free performance. Additionally, a lot number is printed on each container to aid traceability, and the containers are supplied in eight handy bags of 50 (400 containers to a carton). The new containers are available in several varieties, including labeled, unlabeled, irradiated and non-pyrogenic.
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miacom

Rapid test to identify pathogen from blood cultures

Based on fluorescence in situ hybridisation and designed to differentiate Staphylococcus aureus from coagulase-negative Staphylococci in positive blood cultures, the hemoFISH S.aureus/CNS Screen supports clinicians in effectively managing blood stream infections. The test also fits perfectly in today’s laboratory routine. Total turnaround time is only 15 minutes so that results can be reported together with the Gram stain. In addition, up to 12 blood cultures can be processed and analysed simultaneously, allowing microbiologists to apply this test in a batch mode. Importantly, the simple and robust assay procedure, which includes intrinsic controls in every test, is very accurate.Besides the hemoFISH product line, multiplex tests for semi-quantitative identification of pneumoniarelated pathogens directly from respiratory secretions are offered.
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siemens logo

Lactate assay

A lactate assay is now available for Siemens’ recently launched RAPIDPoint 500 system for cartridge-based critical care testing at the point of care. Lactate joins an already extensive assay menu that includes blood gas, electrolytes, metabolites and CO-oximetry. The user-friendly system delivers rapid and accurate test results in approximately 60 seconds. The lactate assay further enhances the system’s functionality for clinicians relying on critical-care testing in, for example, Accident & Emergency departments or Intensive Care Units.
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woodley

System to facilitate diagnosis of diseases in remote areas

Performing a haematology and biochemistry screen in 15 minutes is never normally achieved without sending samples off to a lab, which is virtually impossible in locations such as rural Africa. A health screening package based on dry reagent technology, the revolutionary design of the Insight Diagnostic System will now allow a full haematology, biochemistry and infectious disease profile to be performed within a short time period using just capillary blood at the point of care. The 3-component system combines the SpotChem EZ clinical chemistry analyser, the QBC Autoread Plus haematology analyser and the QBC ParaLens Advance fluorescence microscopy system. The dry reagent technology eliminates many of the issues faced by clinicians relating to storage space, biohazardous waste and spillages. The system does not require any regular servicing or maintenance. The clinical chemistry analyser is easy to use and provides the capability to test a total of 22 biochemistry parameters. The haematology system uses specially designed capillary tubes and can measure nine clinically significant haematology parameters in just seven minutes. Once the haematology process is complete, the same capillary tube containing the patient sample can be immediately examined for infectious disease parasites, including malaria, filariasis and trypanosamiasis, using the fluorescence microscopy system.
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pro lab

Rapid test for norovirus

The number of reported norovirus cases is on the increase, with explosive outbreaks of this highly contagious pathogen leading to acute gastroenteritis. To improve outbreak management and help reduce transmission of the virus, a rapid assay for the detection of norovirus in faecal samples is now available. NOROTOP+ is a qualitative lateral flow assay allowing effective detection in just 15 minutes. This simple visual assay uses specific monoclonal antibodies to allow rapid, one-step detection of norovirus genogroups I and II, offering excellent sensitivity and specificity to facilitate quick and convenient identification and management of outbreaks. The individually packaged test strips can be safely stored at room temperature for up to 12 months, providing a practical and economical solution for norovirus testing whenever the need arises.
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lgc

Range of certified reference materials

Manufactured and certified to ISO Guide 34, using ISO 17025 accredited processes in LGC’s own laboratories, the the LoGiCal range of certified reference materials offers scientists a choice of natural and deuterium labelled compounds, each supplied with a detailed Certificate of Analysis. The certified reference materials fully satisfy national and international labelling and other requirements for transportation, health and safety. The range focuses on the forensic and clinical sectors. Initially providing laboratories with access to over 800 of the most widely used standard reference materials, the new product range will comprise drugs of abuse and prescription drugs in standard solutions and powder format, with stocks maintained locally at LGC Standards international offices to help eliminate delays due to the complex, lengthy import procedures associated with the procurement of controlled substances.
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