Acusera 24•7 (Edit)

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Acusera 24•7 (Edit)

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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?

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    With real-time peer group data, laboratories can instantly compare statistics to other labs using the same lot of QC material.
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    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.

     

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    Automatically calculate %Bias, Total Error and Sigma Metrics, enabling enhanced performance assessment and improved QC strategy design.
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    Acusera 24•7 generates Levey-Jennings, Histogram and Performance Summary Charts for efficient performance monitoring.
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    Designed to speed up the review process, our comprehensive range of easy-to-read reports include: Statistical Metrics, Uncertainty of Measurement and Audit Trails.
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    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.

     

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    Software flexibility allows laboratories to configure their own performance limits, multi-rules, consensus groups and target values for each instrument or QC lot.
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    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)

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RIQAS is the world’s largest External Quality Assessment scheme with more than 47,000 laboratory participants spanning over 139 countries

Why Choose RIQAS?

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    Our rapid, user-friendly reports allow at-a-glance performance assessment.  Complimentary multi-instrument, inter-laboratory and end-of-cycle reports are also available.
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    The availability of large peer groups ensures robust data is available for a wide range of instruments and methods.
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    Consolidate EQA analysis, reduce workload and costs with our comprehensive, multi-parameter programmes.
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    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.
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    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.
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    RIQAS.net is a convenient, cloud based data entry system which allows participants to return results and view reports online.
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    RIQAS programmes are accepted by national and international accreditation bodies including ISO 17043:2010 – “Conformity Assessment – General Requirements for Proficiency Testing”.

     

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    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 EQA 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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RIQAS FAQs

RIQAS Past Panels

RIQAS FAQs

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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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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?

Stemming from RIQAS, the world’s largest External Quality Assessment programme, RIQAS Past Panels* facilitate a series of QC and interlaboratory functions, including:

 

Method Validation

New Instrument Validation

Assay Evaluation

Poor Performance Troubleshooting

Staff Training

Available Panels

Available RIQAS Past Panels* include:

• 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

Support Data Included

All RIQAS Past Panels are provided with an Excel document containing supporting data for the instrument and method of interest.

Multi Level Samples

RIQAS Past Panel samples span multiple levels, making them ideal for ensuring accurate instrument performance across the measuring range.

Comprehensive Reports

RIQAS Past Panels allow laboratories to receive comprehensive external QC reports even after program close.

For more information on RIQAS Past Panel availability or to take part in this EQA scheme, contact us today and speak to one of our friendly and knowledgeable sales representatives. 


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
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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.

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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.

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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.

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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.

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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.

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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. 

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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.

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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.

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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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Quality Controls


Interlaboratory Data Management – July 2019

Contact Us          RIQAS.net Log-in

Acusera 24•7 Live Online is an interlaboratory data management and peer group reporting package complementing the Acusera range of true third party quality controls. Designed to assist in the management of daily QC activities, Acusera 24•7 Live Online will help to meet regulatory requirements, improve error detection, reduce false rejections and ensure accurate patient results.

Delivering an online platform for effective QC data management, our software provides unique access to instantly updated real-time peer group data, automatically generated QC statistics, QC multi-rules, interactive charts and comprehensive reports.

‘The laboratory shall have a procedure to prevent the release of patient results in the event of quality control failure. When the quality control rules are violated and indicate that examination results are likely to contain significant errors the results shall be rejected… Quality Control data shall be reviewed at regular intervals to detect trends in examination performance’.

ISO 15189:2012

Why implement an interlaboratory program?

Acusera 24•7 Live Online is an essential QC tool for laboratories of all sizes. By participating and implementing our software your laboratory will be able to do the following;

  • Quickly identify trends, system errors and reagent issues, minimising expensive repeat tests
  • Automatically calculate Measurement Uncertainty, Total Error and Sigma Metrics
  • Bridge the gap between daily quality control and external quality assessment
  • Improve EQA performance by eliminating any undetected bias
  • Facilitate regulatory compliance
  • Minimise false rejections through the use of QC multi-rules
  • Increase confidence in assigned QC target values
  • Speed up troubleshooting processes, shortening delays in reporting

Acusera 24•7 key features and benefits

Peer group statistics are now uniquely updated live in real-time ensuring immediate access to the most up to date information available while ultimately reducing time and money spent troubleshooting, re-running samples and performing instrument maintenance. Peer groups may be based on worldwide statistics or an affiliate group of laboratories meaning you can instantly discover how you compare to other laboratories using the same lot of QC and identify if issues are unique to your laboratory or a widespread problem.

Available at no extra cost the unique dashboard allows instant identification of any QC failures and from the last seven days. Designed to significantly reduce the time spent analysing data, this highly convenient and user-friendly function means corrective action can be taken immediately with minimum disruption to the laboratory’s output. Alerts are also provided when a control lot is reaching expiry, reducing the risk of using expired material.

Levey-Jennings, Histogram and Performance Summary Charts are generated on demand, delivering quick and easy performance monitoring. With Acusera 24•7 Live Online, users have the ability to add multiple instruments, parameters and lots to a single chart allowing comparative performance assessment and immediate visualisation of any ongoing or emerging trends.

The user-friendly interface and interactive nature of the chart allows you to view data for a specific date range, zoom in on a specific data point, comment on individual data points and record events including calibration and reagent lot changes for enhanced review of trends.

 

Our software now automatically calculates %Bias, Total Error and Sigma metrics, enabling enhanced performance assessment and improved QC strategy design for your laboratory. The added benefit of Uncertainty of Measurement (UM) helps to meet ISO 15189 requirements. In addition results may be rejected or alerted based on QC multi-rules or user defined performance limits including Rilibak, CLIA and biological variation.

The Acusera Advisor tool will conveniently recommend a set of QC multi-rules and a minimum QC frequency for each assay based on previous performance history. Tailoring QC multi-rules to each assay in this way will make QC processes more efficient whilst ensuring high error detection rates.

Designed to help speed up the review process a range of comprehensive reports are available including, Statistical Metrics Reports, Uncertainty of Measurement Report, Exception Report, and the Audit Trail Report which provides a secure, electronic record of the creation, modification and deletion of data. This effective method of documenting the review process can help laboratories meet regulatory requirements and gain accreditation.

 

Evaluate and review any poor performing QC tests

The Data Review report displays data for all QC tests which have fallen outside your laboratory’s user-defined performance limits. Data may be filtered by date, instrument, lot number or rule violation. It may also be filtered to display only alerted/rejected results. The report can be exported or printed easily, to document the review process.

As always, results are colour-coded for added convenience. Once results have been evaluated, managers can record their actions by marking each result as ‘reviewed’. A ‘reviewed’ result will no longer appear on the Dashboard.

Our fully automated connectivity solution is designed to meet the needs of all laboratory types and sizes. QC data can be quickly and efficiently imported from LIMS to Acusera 24•7 Live Online without the need to import files or manually enter data.

  • Reduce workload by eliminating issues associated with manual data entry
  • Increases productivity and efficiency
  • Captures and imports only QC data
  • Secure real-time connection without disruption to the laboratory
  • The software is also capable of bi-directional communication with LIMS

Packages For Customisation

There are several options available for participation in Acusera 24•7, ranging from basic to advanced user options. Click below to learn more.


Randox International Quality Assessment Scheme (RIQAS)

Randox International Quality Assessment Scheme is the world’s largest external quality assessment (EQA) scheme. Currently offering 33 programmes, RIQAS has more than 50,000 laboratory participants in over 139 countries.

RIQAS  | Key Benefits

Click each icon for full benefits
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User-Friendly Reports

Presented in a user-friendly, one page per parameter format, complimentary multi-instrument and interlaboratory RIQAS reports allow comparative performance assessment of all laboratory systems. Each End-of-Cycle report summarises performance compared to the previous cycle, allowing laboratories to identify quality improvement over time.

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Large Database of Users

With 47,000 RIQAS participants in 139 countries worldwide, a large peer group means more information is available for a wide range of instruments and methods. This therefore ensures greater accuracy and confidence, while reducing the level of uncertainty in results used for comparison.

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Consolidation

Comprising over 360 parameters across 33 comprehensive EQA programmes, RIQAS can streamline external quality assessment by significantly reducing the number of individual programmes needed. Consolidation is guaranteed to save laboratory time and money, with fewer samples to prepare, reports to interpret and number of kits to store.

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Report Frequency

Frequent reporting allows early identification of test system errors and implementation of any necessary corrective actions with minimum disruption to the lab, reducing costly errors with patient results. RIQAS offers bi-weekly, monthly, and quarterly options (programme specific), with a turnaround of less than 72 hours for most reports.

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Flexibility

With 33 flexible external quality assessment programmes available, RIQAS is suitable for every laboratory. Reduced parameter and reporting options are available for selected programmes, with the ability to register up to 5 instruments per programme at no extra cost this will help save money and facilitate comparative performance assessment.

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Result Entry

RIQAS.Net is a convenient, cloud based data entry system which allows participants to return results and view reports online in seconds. Participants can submit results directly into the online RIQAS database, where PDF reports are collated and emailed back to participants. Current and previous reports are available to download at anytime, ideal for on the go users.

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Accredited

RIQAS programmes are accepted by national and international accreditation bodies worldwide, including ISO 17043:2010 – ‘Conformity Assessment – General Requirements for Proficiency Testing’. This guarantees high quality programmes that are fit for purpose and assist laboratories in achieving their own accreditation.

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Quality Material

Every RIQAS sample is manufactured to the highest standard, spanning clinically relevant levels to allow identification of concentration related biases to ensure accurate instrument performance across the entire analytical range. Designed to be commutable, RIQAS samples are manufactured from human source material and are free from interfering preservatives, increasing confidence that performance mirrors that of patient samples.

RIQAS EQA Programmes

Choice and flexibility guaranteed with 33 programmes available.

RIQAS EQA Reports

User-friendly, one page reports available for each parameter.

*Please note, product availability may vary country to country.

More About RIQAS

What is External Quality Control?

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.

Why Participate in an EQA Scheme?

Ideal Specifications of an EQA Provider

Large Database of Users

Large participation numbers

Liquid ready

Blind samples

RIQAS - Stable and consistent sample matrix

Stable and consistent sample matrix

Frequency

Frequent analysis

Highly Accredited

International accreditation

User-Friendly Reports

Detailed reports

RIQAS - Realitic range of analyte concentrations

Realistic range of analyte concentrations

RIQAS - sample matirx similar to patient sample

Samples react in the sample manner as patient samples

RIQAS - rapid feedback

Rapid feedback

Want to know more?

Get in touch or download our full RIQAS brochure

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RIQAS FAQs

RIQAS Past Panels

Quality Controls

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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.

(Click to enlarge)

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.

(Click to enlarge)


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.

  1. If a participant’s result matches the target category then they will receive the score of 0 and the comment “acceptable” given.
  2. 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.
  3. 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:

  1. Target Category, which is dependent on the unit registered
  2. The result which has returned by the participant
  3. The score achieved for the current sample
  4. The comment of Acceptable / Unacceptable / Borderline
  5. Where the comment is “Unacceptable” it is highlighted in bold italics and underlined
  6. 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.

(Click to enlarge)

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.

(Click to enlarge)


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