Acusera 24.7 Software Update
Acusera 24.7 Software Update
The latest update of Acusera 24.7 has officially launched, allowing RX Imola, RX Modena and RX Daytona+ users to import compatible QC data files from a configured analyser to Acusera
Acusera 24•7 | Update Features
Our brand new Acusera 24.7 video is here! Take a look now
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Acusera 24•7 (Edit)
Designed to complement our range of true third party controls, Acusera 24•7 is a live, cloud based interlaboratory data management and peer group reporting software, intended to assist in the management of daily QC activities.
Why implement an interlaboratory program?
- With real-time peer group data, laboratories can instantly compare statistics to other labs using the same lot of QC material.
- Acusera 24•7 boasts a unique dashboard, allowing for instant identification of any QC failures over the past seven days and alerts of product expiry.
- Automatically calculate %Bias, Total Error and Sigma Metrics, enabling enhanced performance assessment and improved QC strategy design.
- Acusera 24•7 generates Levey-Jennings, Histogram and Performance Summary Charts for efficient performance monitoring.
- Designed to speed up the review process, our comprehensive range of easy-to-read reports include: Statistical Metrics, Uncertainty of Measurement and Audit Trails.
- Automated upload of QC data direct to Acusera 24•7 via LIMS and Middleware is available. This function eliminates the need for manual data entry further increasing efficiency.
- Software flexibility allows laboratories to configure their own performance limits, multi-rules, consensus groups and target values for each instrument or QC lot.
- This cloud based software is available for laboratories to access anytime, anywhere therefore eliminating the need for installation, software maintenance and frequent back ups.
Why implement an interlaboratory program?
Randox International Quality Assessment Scheme (RIQAS)
RIQAS is the world’s largest External Quality Assessment scheme with more than 50,000 laboratory participants spanning over 139 countries
Why Choose RIQAS?
- Our rapid, user-friendly reports allow at-a-glance performance assessment. Complimentary multi-instrument, inter-laboratory and end-of-cycle reports are also available.
- The availability of large peer groups ensures robust data is available for a wide range of instruments and methods.
- Consolidate EQA analysis, reduce workload and costs with our comprehensive, multi-parameter programmes.
- Frequent reporting allows early identification of test system errors, while our 72 hour report turnaround enables corrective action to be taken with minimum disruption to the lab.
- Flexible programme options are available to suit all laboratory budgets. The option to register up to 5 instruments per programme at no extra fee further reduces costs and facilitates comparative performance assessment.
- RIQAS.net is a convenient, cloud based data entry system which allows participants to return results and view reports online.
- RIQAS programmes are accepted by national and international accreditation bodies including ISO 17043:2010 – “Conformity Assessment – General Requirements for Proficiency Testing”.
- EQA samples are manufactured to the highest quality standard and span clinically relevant levels. A commutable sample matrix increases confidence that performance mimics that of patient samples.
RIQAS EQA Programmes
Choice & flexibility are guaranteed with our 33 programme portfolio.
Browse the programmes below
RIQAS EQA Reports
User-friendly, one-page per parameter reports allow for at-a-glance performance assessment.
Browse the reports below.
Ideal specifications of an External Quality Assessment provider
External Quality Assessment retrospectively assesses performance against other laboratories using the same method and instrument, by analysing “blind” samples as if they were patient samples. Results are frequently submitted for statistical analysis, following which each lab will receive an overall comparative report. Find out why EQA is important here.
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Acusera 24.7 Software Update
The latest update of Acusera 24.7 allows RX Imola, Modena and Daytona+ users to import compatible QC files from a configured analyser to Acusera 24.7 without the need for manipulation. This new functionality eliminates the need for manual data entry, therefore effectively reducing the risk of transcription errors whilst speeding up the reporting process.
Acusera 24•7 | Update Features
Our brand new Acusera 24.7 video is here! Take a look now
Want to know more?
Contact us or download our Acusera 24.7 brochure today.
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Acusera 24.7 FAQs
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Quality Controls
RIQAS Past Panels
RIQAS (Randox International Quality Assessment Scheme) is the largest global EQA scheme with over 50,000 participants in more than 139 countries. Our range currently comprises 33 programmes and the majority of clinical testing.
What are RIQAS Past Panels?
Available Panels
• Ammonia/ Ethanol
• Anti-TSH Receptor
• Blood Gas
• BNP
• Cardiac
• Cerebrospinal Fluid (CSF)
• Clinical Chemistry
• Coagulation
• CO-Oximetry
• CYFRA 21-1
• ESR
• Glycated Haemoglobin (HbA1c)
• Haematology
• Human Urine
• Immunoassay
• Immunoassay Speciality 1
• Immunoassay Speciality 2
• Immunosuppressant Drugs
• Lipid
• Liquid Cardiac
• Maternal Screening
• Serology Epstein Barr Virus (EBV)
• Serology (HIV/ Hepatitis)
• Serology (Syphilis)
• Serology (ToRCH)
• Specific Proteins
• Sweat Testing
• Therapeutic Drugs
• Trace Elements in Blood
• Trace Elements in Serum
• Trace Elements in Urine
• Urinalysis
• Urine Toxicology
*Product availability is dependent on RIQAS stock surplus levels.
Benefits of RIQAS Past Panels
All RIQAS Past Panels are provided with an Excel document containing supporting data for the instrument and method of interest.
RIQAS Past Panel samples span multiple levels, making them ideal for ensuring accurate instrument performance across the measuring range.
RIQAS Past Panels allow laboratories to receive comprehensive external QC reports even after program close.
Acusera 24.7
Designed to complement our range of Acusera true third party controls, Acusera 24•7 is a live, cloud based interlaboratory data management and peer group reporting software, intended to assist in the management of daily QC activities.
Why implement an interlaboratory program?
Acusera 24•7 | Key Features and Benefits
Click each icon for full features and benefits
Peer Group Statistics
With real-time peer group data, laboratories can instantly compare statistics to other labs using the same lot of QC material. Data is continuously updated, allowing labs to identify unique and widespread issues to help reduce time and money spent on troubleshooting, re-running samples and performing instrument maintenance.
Unique Dashboard Interface
Acusera 24•7 boasts a unique dashboard, allowing for instant identification of any QC failures over the past seven days and alerts of product expiry. The interface is designed to reduce the time spent analysing data, meaning corrective action can be taken immediately with minimum disruption to laboratory output.
Advanced Statistical Analysis
Automatically calculate %Bias, Total Error and Sigma Metrics, enabling enhanced performance assessment and improved QC strategy design. Reject or alert data based on QC multi-rules or user defined performance limits including Rilibak, CLIA and biological variation. Uncertainty of Measurement (UM) is also calculated, helping meet ISO 15189 requirements.
Fully Interactive Charts
Acusera 24•7 generates Levey-Jennings, Histogram and Performance Summary Charts for efficient performance monitoring. Users can add multiple instruments, parameters and lots to a single chart to compare performance and assess emerging trends. Laboratories can review data for date ranges, explore individual data points and record events.
Comprehensive Reports
Designed to speed up the review process, our comprehensive range of easy-to-read reports include: Statistical Metrics Reports, Uncertainty of Measurement Report, Exception Report, and an Audit Trail Report. Reports can be customised for specific date ranges and filtered to display individual test or instrument data.
Automated Data Import
This optional software allows for automated upload of QC data direct to Acusera 24•7 via LIMS and Middleware. This function eliminates the need for manual data entry, further saving costs and increasing efficiency.
Highly Flexible
Software flexibility allows laboratories to configure their own performance limits, multi-rules, consensus groups and target values for each instrument or QC lot. This software’s internal functions can be used with any manufacturer’s QC material.
24/7 Access
This cloud based software is available for laboratories to access anytime, anywhere therefore eliminating the need for installation, software maintenance and frequent back ups. Access Acusera 24•7 here.
Technical Support
With Acusera 24•7, expert technical support is available from our team of highly trained specialists. Laboratories can remotely access the technical support service for immediate troubleshooting, therefore eliminating the need for on-site assistance.
Want to know more?
Contact us or download our Acusera 24.7 brochure today.
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RIQAS Serology Report
The Serology report is available within ten days of the final submission date. The results for each parameter are displayed on a single page report. There are two types of Serology report – one for qualitative reporting and one for quantitative reporting. Each of these report ensure quick and easy performance assessment.
RIQAS EQA Reports
The Qualitative report comprises three subsections including a text section, Histogram and method summary. The text section conveniently displays your laboratory’s result to the correct result for your method. The Histogram visually displays your laboratory’s result in relation to all of the results submitted for your method group and the all method group. Finally, the method summary provides a breakdown of the results for all methods registered with RIQAS.
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The Quantitative report comprises four subsections including a text section, Histogram, Levey-Jennings chart and method summary. The text section conveniently displays your laboratory’s result to the mean for comparison, the histogram visually displays your laboratory’s result to the mean for comparison, the Levey-Jennings chart displays the SD for the last 20 samples ensuring instant identification of performance over time and finally the method summary provides a breakdown of the results submitted for all methods registered with RIQAS.
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RIQAS Urinalysis Report
RIQAS Urinalysis reports have been designed specifically for participants of the RIQAS Urinalysis programme (RQ9138). Report features include;
- Scoring system
- Ability to rate performance and visualise historical performance data
- Visual representation of performance
- Peer group comparison levels
To find out more on the range of features available with the report, see the table below.
RIQAS EQA Reports
The Urinalysis Report scoring system, scores participants based on a spread of results over each category and how far a participant is away from the consensus, which is referred to as the Target Category.
The score calculated is based on how close to the target category a participant’s result falls. A score of 0 refers to a result which falls within the target category and therefore, the comment “acceptable” will be given. A laboratory’s performance is described as being acceptable or unacceptable based on this calculated score.
A laboratory must achieve a score of between -6 and +6 for their performance to be deemed acceptable. Scores can fall between the values of -10 and +8.
- If a participant’s result matches the target category then they will receive the score of 0 and the comment “acceptable” given.
- Where a participant returns a negative result and the target category is positive (category 9), the participant score will be -10. The comment “unacceptable” will be given.
- Where a participant returns a positive result (category 9) and the target category is negative, the participant score will be +8 and the comment “unacceptable” given.
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Current Sample
The score achieved for the current reported sample together with the associated comment of acceptable, unacceptable or borderline will be listed in the comments box located towards the top of the results page for each registered parameter. The percentage (%) of results from the selected peer group which fall within the target category are also stated.
Potential Historical Information
The number of correct scores (i.e. scores of 0) that have been submitted in the last “n” samples, up to a maximum of 6 previous samples. The number of acceptable assessments that have been submitted in the last “n” samples, up to a maximum of 6 previous samples.
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Charting of Current & Historical Information
Results of scoring for each sample are displayed on a Levey-Jennings style chart with “0” score in the middle and scoring categories positioned on either side for 2, 4, 6, 8 and 10. The chart is shaded into bands depending on the scores.
Acceptable scores (0-6) have no shading, Borderline scores (6-8) have light red shading and unacceptable scores (8-10) are shaded a darker red.
Scores for each of the last 12 samples are plotted against the appropriate sample number and the chart also indicates whether the participant’s reported result category is higher or lower than the target category.
The target categories are stated along the top of the chart and if there are no target categories due to a lack of numbers then an “X” is plotted to show that a result has been submitted but could not be scored.
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Reporting – Summary Page
The summary page at the end of the report lists all of the parameters that a participant has registered for.
For each parameter the following information is stated:
- Target Category, which is dependent on the unit registered
- The result which has returned by the participant
- The score achieved for the current sample
- The comment of Acceptable / Unacceptable / Borderline
- Where the comment is “Unacceptable” it is highlighted in bold italics and underlined
- The number of “Acceptable” assessments that have been achieved over the previous 6 samples
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RIQAS Urine Toxicology Report
A dedicated report is provided for the Urine Toxicology programme. The report is divided into two subsections; the screening (qualitative) and the quantitative section, allowing for visual performance assessment at-a-glance.
RIQAS EQA Reports
Your laboratory’s result is displayed along with the correct response. A visual chart is also provided displaying performance of the last 20 samples. A breakdown of the screening results submitted by other laboratories in your method group and all method groups for the current sample is also provided at a variety of cut-offs. A further breakdown is provided for various methods at your specific cut-off.
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The Quantitative section of the Urine Toxicology report is further broken down into a text section comparing your laboratory’s performance to the mean for comparison, a Histogram chart indicating your laboratory’s performance in relation to the method group and the all method group and a multi-method section highlighting the performance of other methods.
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RIQAS Instrument Group Report
All RIQAS participants are entitled to register up to five separate instruments per programme at no extra cost.
Individual reports for each instrument are supplied as normal in addition to a complimentary instrument group report allowing the performance of each instrument to be uniquely compared and assessed easily.
RIQAS EQA Reports
The multi-instrument group report displays the %Deviation for the last 10 samples along with the RM%Dev across all registered laboratory instruments. The %Dev for each instrument is plotted on a user-friendly, colour coded chart for instant identification of poor performing instruments.
As an ISO requirement, the Multi-Instrument Report is an extremely useful and beneficial tool for laboratories – “Laboratories with two or more analysers for examinations, should have a defined mechanism for comparison of results across analysers” – ISO 15189:2012.
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