Our Acusera Linearity Sets are perfect for laboratories wishing to challenge the full reportable range of their instruments. With sets available for Roche & Beckman analysers, our sets are sure to meet all your laboratory and regulatory requirements.
Randox QC offer an extensive range of third party quality controls. Manufactured independently, the Acusera range delivers unbiased performance assessment with any instrument or method, helping to meet ISO 15189:2012 requirements whilst simultaneously eliminating the need for multiple instrument dedicated controls.
Quality Control for Point of Care Testing - White PaperRandox
Point of care testing (POCT) refers to testing that is performed near or at the site of a patient with the result leading to a possible change in the care of the patient. Over the past few years, the popularity and demand of POCT has been growing rapidly. This should come as no surprise as there are many advantages to POCT, for example, the added convenience of being able to obtain a rapid result at the patient’s bedside, thus allowing immediate action, saving time and improving the potential outcome for the patient.
The document describes Randox's Acusera line of third party quality control products. It provides details on their blood gas controls, antioxidant controls, benefits of consolidation, and commitment to quality. The blood gas controls come in three levels and test for 10 parameters. The antioxidant controls include tests for glutathione reductase, glutathione peroxidase, superoxide dismutase, and total antioxidant status. Acusera controls offer benefits such as commutability, accurate target values, consolidation of multiple competitor controls into single controls, and clinically relevant analyte levels. Randox is committed to quality and has received various accreditations.
QC Multi rules - Improving Laboratory Performance Through Quality ControlRandox
Randox Quality Control's latest educational guide examines and explains what QC Multi-Rules are, How to identify an out of control event with QC rules, How to use QC Multi-Rules, The different types of analytical errors, The tools to assist labs and how a lab can troubleshoot QC errors.
Third party quality controls are important to ensure accurate patient test results. They provide an independent assessment of analytical performance compared to controls from instrument or reagent manufacturers. The document describes several examples where Randox third party controls detected errors that dedicated manufacturer controls failed to identify, including instrument faults, procedural errors, and shifts in results between reagent batches. Regulatory bodies recommend using third party controls over manufacturer controls to independently monitor testing quality.
Acusera Third Party Quality Controls for Medical Laboratories Randox
Randox is a leading provider of true third party quality controls for laboratories. Their controls offer the most accurate target values based on data from over 23,000 labs, the most consistent material between lots, and unrivalled stability that meets or exceeds claims. Many controls are 100% human material, important for immunoassay methods. As true third party controls, they provide an unbiased assessment of performance across different instruments and methods, reducing the need for multiple controls. Randox controls also allow for consolidation, reducing the number of individual controls required through their wide coverage of analytes.
This document discusses different quality control formats that laboratories can use to ensure accurate patient test results. It describes the benefits of consolidated multi-analyte controls that allow laboratories to reduce costs by using fewer control products and simplify the quality control process. These controls consolidate parameters into single vials containing up to 100 analytes. The document also discusses liquid ready-to-use controls as being the most convenient format that require no preparation or reconstitution. Finally, it promotes Randox quality control products and services that aim to streamline quality control testing for laboratories.
Randox QC offer an extensive range of third party quality controls. Manufactured independently, the Acusera range delivers unbiased performance assessment with any instrument or method, helping to meet ISO 15189:2012 requirements whilst simultaneously eliminating the need for multiple instrument dedicated controls.
Quality Control for Point of Care Testing - White PaperRandox
Point of care testing (POCT) refers to testing that is performed near or at the site of a patient with the result leading to a possible change in the care of the patient. Over the past few years, the popularity and demand of POCT has been growing rapidly. This should come as no surprise as there are many advantages to POCT, for example, the added convenience of being able to obtain a rapid result at the patient’s bedside, thus allowing immediate action, saving time and improving the potential outcome for the patient.
The document describes Randox's Acusera line of third party quality control products. It provides details on their blood gas controls, antioxidant controls, benefits of consolidation, and commitment to quality. The blood gas controls come in three levels and test for 10 parameters. The antioxidant controls include tests for glutathione reductase, glutathione peroxidase, superoxide dismutase, and total antioxidant status. Acusera controls offer benefits such as commutability, accurate target values, consolidation of multiple competitor controls into single controls, and clinically relevant analyte levels. Randox is committed to quality and has received various accreditations.
QC Multi rules - Improving Laboratory Performance Through Quality ControlRandox
Randox Quality Control's latest educational guide examines and explains what QC Multi-Rules are, How to identify an out of control event with QC rules, How to use QC Multi-Rules, The different types of analytical errors, The tools to assist labs and how a lab can troubleshoot QC errors.
Third party quality controls are important to ensure accurate patient test results. They provide an independent assessment of analytical performance compared to controls from instrument or reagent manufacturers. The document describes several examples where Randox third party controls detected errors that dedicated manufacturer controls failed to identify, including instrument faults, procedural errors, and shifts in results between reagent batches. Regulatory bodies recommend using third party controls over manufacturer controls to independently monitor testing quality.
Acusera Third Party Quality Controls for Medical Laboratories Randox
Randox is a leading provider of true third party quality controls for laboratories. Their controls offer the most accurate target values based on data from over 23,000 labs, the most consistent material between lots, and unrivalled stability that meets or exceeds claims. Many controls are 100% human material, important for immunoassay methods. As true third party controls, they provide an unbiased assessment of performance across different instruments and methods, reducing the need for multiple controls. Randox controls also allow for consolidation, reducing the number of individual controls required through their wide coverage of analytes.
This document discusses different quality control formats that laboratories can use to ensure accurate patient test results. It describes the benefits of consolidated multi-analyte controls that allow laboratories to reduce costs by using fewer control products and simplify the quality control process. These controls consolidate parameters into single vials containing up to 100 analytes. The document also discusses liquid ready-to-use controls as being the most convenient format that require no preparation or reconstitution. Finally, it promotes Randox quality control products and services that aim to streamline quality control testing for laboratories.
Acusera 24.7 Interlaboratory Data Management - June 17 LT244Randox
Acusera 24.7 Live Online version 2.0 is here! Faster, smarter and more efficient than ever before, this interlaboratory data management program will be sure to help streamline internal QC in all laboratories regardless of size.
This document provides a guide to running quality control (QC) samples in a laboratory. It outlines the steps for receipt and storage of QC materials, including recommended temperature conditions. It describes safe handling practices and preparation steps for different types of controls, such as liquid ready-to-use, liquid frozen, and lyophilized controls. The guide also covers the application and interpretation of QC results to ensure test values fall within the expected ranges listed on the product insert. Following the procedures outlined helps ensure proper QC monitoring of analytical testing in the laboratory.
This document describes a human liquid ready-to-use stable multi-analyte control containing 27 different analytes including antibody isotypes, complement components, and other specific proteins. It reports that the control material has an open vial stability of 30 days when stored between 2-8 degrees Celsius and a shelf life stability of at least 2 years under the same storage conditions based on measurements on various automated systems. The control is concluded to be a convenient ready-to-use material for clinical applications that standardizes the test menu and reduces errors.
Designing an appropriate qc design procedure for your lab 5 mar15Randox
This document discusses the importance of quality control (QC) procedures in laboratories and provides five simple steps for effective QC. It emphasizes that the goal of QC is to ensure accurate and reliable test results in order to avoid harming patients. The five steps include: 1) identifying quality specifications for each test, 2) choosing good quality control materials, 3) starting and ending patient testing with QC evaluation, 4) understanding good QC results, and 5) recognizing and addressing out-of-control events. Participation in an external quality assessment scheme is also recommended to help detect errors. The document stresses applying QC procedures appropriately based on each test's performance and prioritizing high-risk tests.
Improving Laboratory Performance Through QC - CommutabilityRandox
This document discusses the importance of using commutable quality control materials in laboratories. It states that approximately 70% of clinical decisions are based on laboratory test results, so reliable quality control is needed. Non-commutable controls can lead to unnecessary shifts in quality control values when reagent batches change. In contrast, commutable controls will perform consistently and reflect actual patient sample performance. The document also describes a case study that demonstrates how a laboratory's quality control values remained stable between reagent batch changes when using Randox commutable controls, unlike with their previous non-commutable controls.
RIQAS External Quality Assessment for Medical Laboratories Randox
RIQAS (Randox International Quality Assessment Scheme) is the world's largest global EQA provider serving over 24,000 laboratory participants in more than 105 countries. Our comprehensive programme offering covers a wide range of routine and esoteric analytes enabling laboratories to significantly reduce the number of programmes they participate in while helping to reduce costs at the same time.
More than 24,000 laboratory participants
Present in over 105 countries
22 flexible EQA programmes
Cost effective options to suit all labs
Accredited to ISO/IEC17043:2010
Frequent analysis with rapid feedback
User friendly yet comprehesive reports
End-of-cycle reports provided
Submit results and view reports online via RIQAS.net
Register up to five analysers per programme at no extra cost
Improving Laboratory Performance Through Quality Control - The role of EQA in...Randox
Randox Quality Control's five simple steps to QC success. The second education guide from Randox QC for clinical laboratory staff. The guide will examine how EQA works, benefits of EQA and what a laboratory should look for when choosing an EQA scheme.
RIQAS is the largest international External Quality Assessment (EQA)/ Proficiency Testing (PT) scheme, there are currently more than 45,000 participants in 133 countries.
Acusera 24.7 Interlaboratory Data Management Randox
Acusera 24•7 Live Online is an interlaboratory data management package designed to complement the Acusera range of Internal Quality Controls. Created to help laboratories effectively manage and interpret their QC results, the analytical capabilities of Acusera 24•7 Live Online, coupled with the superior quality and flexibility of our Acusera control range, will revolutionise your laboratory's workflow enabling early identification of any trends or system errors.
Acusera 24.7 Live Online will automatically calculate internal QC statistics including mean, standard deviation and CV. The ability to apply user defined QC multi-rules will help to reduce false rejections and maintain a high level of error detection.
Online access anytime, anywhere
Peer group data from over 20,000 participants
Peer group statistics updated daily
Unique dashboard highlights poor performance
Interactive charts combining multiple analytes, lots and instruments
Comprehensive reports including audit trail reports to aid accreditation
Automated QC result entry via Acusera 24•7 Connect
Acusera 24.7 is an interboratory data management software capable of automatically calculating measurement of uncertainty and six-sigma. With real time peer group updates and user friendly comprehensive charts and reports including Levey Jennings and histograms, our Acusera 24.7 software is now smarter, faster and more efficient than ever before!
This document discusses linearity verification materials from Randox. It provides an overview of the product portfolio, which includes solutions for assessing linearity of cardiac markers, specific proteins, and therapeutic drugs on various analyzer platforms. The linearity materials are supplied in a liquid ready-to-use format for convenience. The document also highlights the data reduction software, which automatically generates reports and allows real-time review of peer group data through an intuitive interface.
Designing an appropriate QC procedure for your laboratoryRandox
Improving Laboratory Performance Through Quality Control - Five Simple Steps for QC Success.
It is easy to get caught up in an abundance of QC statistics and forget the fundamental reason why
QC exists in the first instance. QC is about detecting errors and ensuring that the results you
produce are accurate and reliable. All QC procedures should focus on reducing the risk of harm
to the patient. We are not examining statistics; we are examining real patients, real results and real
lives. Around 70% of all medical decisions are based on laboratory results, which is why it is of
utmost importance that each and every laboratory, has a well-designed QC procedure in place.
The laboratory shall determine measurement uncertainty for each measurement procedure,
in the examination phases used to report measured quantity values on patients’ samples. The
laboratory shall define the performance requirements for the measurement uncertainty of each
measurement procedure and regularly review estimates of measurement uncertainty.
QC Multi-rules are designed and used to minimise false rejections and maintain a high rate of error detection. There are six main rules used to determine if results from a run of patient samples should be accepted or rejected, based on the performance of control materials against the rule criteria. Different combinations can be applied depending on the number of controls in use, total allowable error and the instrument in use. The flow chart below is often used to determine if a run should be accepted or rejected.
How often is Right for Laboratory Quality Control?Randox
Improving Laboratory Performance Through QC - How often is right for QC? Ask the Right Questions to get the Right Answers.
It is widely accepted that laboratories should perform QC at least every day of patient testing. However, is this adequate for every assay and for every laboratory? Is running QC once per day really sufficient? what is the "right" frequency for running QC samples in your laboratory?
How to establish QC reference ranges - Randox QC Educational GuideRandox
Establishing QC reference ranges is an important aspect of laboratory quality. Find out how to effectively set reference ranges with our educational guide.
Monitoring External Quality Assessment / Proficiency Testing Performance - Investigating the source of the problem.
In order to identify the source of the problem it is useful to be aware of the most common causes of poor EQA performance. Errors can occur at any
stage of the testing process however EQA is most concerned with detecting analytical errors i.e. errors that occur during the analysis of the sample.
Most analytical errors can be easily divided into three main areas; clerical errors, systematic errors and random errors. Systematic errors result in
inaccurate results that consistently show a positive or negative bias. Random errors on the other hand affect precision and result in fluctuations in
either direction.
Basic QC Statistics - Improving Laboratory Performance Through Quality Contro...Randox
Randox Quality Control's latest educational guide examines Internal Quality Control, External Quality Assessment, Why laboratories should run QC, How often laboratories should run QC, Basic QC statistics and the quality control process.
Understanding statistics in laboratory quality controlRandox
This document discusses laboratory quality control and interpreting quality control results. It outlines a 5 step process: 1) Calculate the mean, 2) Calculate the standard deviation, 3) Establish decision limits, 4) Create a Levey-Jennings chart, and 5) Accept or reject results based on quality control rules. Statistics like the mean, standard deviation, and decision limits are used to monitor the accuracy and precision of analytical testing and ensure reliable patient results. Quality control software can automate the calculation of these statistics and generation of charts to more easily monitor performance.
The RX monaco is a fully automated clinical chemistry analyzer capable of performing 170 tests per hour. It has a discrete, random access design and features include a large test menu, quality control capabilities, intuitive Windows-based software, and remote diagnostics. The analyzer provides cost-effective and reliable testing for small to medium sized clinical laboratories.
The CBC machine is a common diagnostic tool used by doctors to measure a patient's red blood cell count, white blood cell count and platelet count. The machine uses a small sample of the patient's blood, which is then placed into special tubes and analyzed. The results of the analysis are then displayed on a screen for the doctor to review. The CBC machine is an important tool for diagnosing various conditions, such as anemia, infection and leukemia. It can also help to monitor a patient's response to treatment.
Acusera 24.7 Interlaboratory Data Management - June 17 LT244Randox
Acusera 24.7 Live Online version 2.0 is here! Faster, smarter and more efficient than ever before, this interlaboratory data management program will be sure to help streamline internal QC in all laboratories regardless of size.
This document provides a guide to running quality control (QC) samples in a laboratory. It outlines the steps for receipt and storage of QC materials, including recommended temperature conditions. It describes safe handling practices and preparation steps for different types of controls, such as liquid ready-to-use, liquid frozen, and lyophilized controls. The guide also covers the application and interpretation of QC results to ensure test values fall within the expected ranges listed on the product insert. Following the procedures outlined helps ensure proper QC monitoring of analytical testing in the laboratory.
This document describes a human liquid ready-to-use stable multi-analyte control containing 27 different analytes including antibody isotypes, complement components, and other specific proteins. It reports that the control material has an open vial stability of 30 days when stored between 2-8 degrees Celsius and a shelf life stability of at least 2 years under the same storage conditions based on measurements on various automated systems. The control is concluded to be a convenient ready-to-use material for clinical applications that standardizes the test menu and reduces errors.
Designing an appropriate qc design procedure for your lab 5 mar15Randox
This document discusses the importance of quality control (QC) procedures in laboratories and provides five simple steps for effective QC. It emphasizes that the goal of QC is to ensure accurate and reliable test results in order to avoid harming patients. The five steps include: 1) identifying quality specifications for each test, 2) choosing good quality control materials, 3) starting and ending patient testing with QC evaluation, 4) understanding good QC results, and 5) recognizing and addressing out-of-control events. Participation in an external quality assessment scheme is also recommended to help detect errors. The document stresses applying QC procedures appropriately based on each test's performance and prioritizing high-risk tests.
Improving Laboratory Performance Through QC - CommutabilityRandox
This document discusses the importance of using commutable quality control materials in laboratories. It states that approximately 70% of clinical decisions are based on laboratory test results, so reliable quality control is needed. Non-commutable controls can lead to unnecessary shifts in quality control values when reagent batches change. In contrast, commutable controls will perform consistently and reflect actual patient sample performance. The document also describes a case study that demonstrates how a laboratory's quality control values remained stable between reagent batch changes when using Randox commutable controls, unlike with their previous non-commutable controls.
RIQAS External Quality Assessment for Medical Laboratories Randox
RIQAS (Randox International Quality Assessment Scheme) is the world's largest global EQA provider serving over 24,000 laboratory participants in more than 105 countries. Our comprehensive programme offering covers a wide range of routine and esoteric analytes enabling laboratories to significantly reduce the number of programmes they participate in while helping to reduce costs at the same time.
More than 24,000 laboratory participants
Present in over 105 countries
22 flexible EQA programmes
Cost effective options to suit all labs
Accredited to ISO/IEC17043:2010
Frequent analysis with rapid feedback
User friendly yet comprehesive reports
End-of-cycle reports provided
Submit results and view reports online via RIQAS.net
Register up to five analysers per programme at no extra cost
Improving Laboratory Performance Through Quality Control - The role of EQA in...Randox
Randox Quality Control's five simple steps to QC success. The second education guide from Randox QC for clinical laboratory staff. The guide will examine how EQA works, benefits of EQA and what a laboratory should look for when choosing an EQA scheme.
RIQAS is the largest international External Quality Assessment (EQA)/ Proficiency Testing (PT) scheme, there are currently more than 45,000 participants in 133 countries.
Acusera 24.7 Interlaboratory Data Management Randox
Acusera 24•7 Live Online is an interlaboratory data management package designed to complement the Acusera range of Internal Quality Controls. Created to help laboratories effectively manage and interpret their QC results, the analytical capabilities of Acusera 24•7 Live Online, coupled with the superior quality and flexibility of our Acusera control range, will revolutionise your laboratory's workflow enabling early identification of any trends or system errors.
Acusera 24.7 Live Online will automatically calculate internal QC statistics including mean, standard deviation and CV. The ability to apply user defined QC multi-rules will help to reduce false rejections and maintain a high level of error detection.
Online access anytime, anywhere
Peer group data from over 20,000 participants
Peer group statistics updated daily
Unique dashboard highlights poor performance
Interactive charts combining multiple analytes, lots and instruments
Comprehensive reports including audit trail reports to aid accreditation
Automated QC result entry via Acusera 24•7 Connect
Acusera 24.7 is an interboratory data management software capable of automatically calculating measurement of uncertainty and six-sigma. With real time peer group updates and user friendly comprehensive charts and reports including Levey Jennings and histograms, our Acusera 24.7 software is now smarter, faster and more efficient than ever before!
This document discusses linearity verification materials from Randox. It provides an overview of the product portfolio, which includes solutions for assessing linearity of cardiac markers, specific proteins, and therapeutic drugs on various analyzer platforms. The linearity materials are supplied in a liquid ready-to-use format for convenience. The document also highlights the data reduction software, which automatically generates reports and allows real-time review of peer group data through an intuitive interface.
Designing an appropriate QC procedure for your laboratoryRandox
Improving Laboratory Performance Through Quality Control - Five Simple Steps for QC Success.
It is easy to get caught up in an abundance of QC statistics and forget the fundamental reason why
QC exists in the first instance. QC is about detecting errors and ensuring that the results you
produce are accurate and reliable. All QC procedures should focus on reducing the risk of harm
to the patient. We are not examining statistics; we are examining real patients, real results and real
lives. Around 70% of all medical decisions are based on laboratory results, which is why it is of
utmost importance that each and every laboratory, has a well-designed QC procedure in place.
The laboratory shall determine measurement uncertainty for each measurement procedure,
in the examination phases used to report measured quantity values on patients’ samples. The
laboratory shall define the performance requirements for the measurement uncertainty of each
measurement procedure and regularly review estimates of measurement uncertainty.
QC Multi-rules are designed and used to minimise false rejections and maintain a high rate of error detection. There are six main rules used to determine if results from a run of patient samples should be accepted or rejected, based on the performance of control materials against the rule criteria. Different combinations can be applied depending on the number of controls in use, total allowable error and the instrument in use. The flow chart below is often used to determine if a run should be accepted or rejected.
How often is Right for Laboratory Quality Control?Randox
Improving Laboratory Performance Through QC - How often is right for QC? Ask the Right Questions to get the Right Answers.
It is widely accepted that laboratories should perform QC at least every day of patient testing. However, is this adequate for every assay and for every laboratory? Is running QC once per day really sufficient? what is the "right" frequency for running QC samples in your laboratory?
How to establish QC reference ranges - Randox QC Educational GuideRandox
Establishing QC reference ranges is an important aspect of laboratory quality. Find out how to effectively set reference ranges with our educational guide.
Monitoring External Quality Assessment / Proficiency Testing Performance - Investigating the source of the problem.
In order to identify the source of the problem it is useful to be aware of the most common causes of poor EQA performance. Errors can occur at any
stage of the testing process however EQA is most concerned with detecting analytical errors i.e. errors that occur during the analysis of the sample.
Most analytical errors can be easily divided into three main areas; clerical errors, systematic errors and random errors. Systematic errors result in
inaccurate results that consistently show a positive or negative bias. Random errors on the other hand affect precision and result in fluctuations in
either direction.
Basic QC Statistics - Improving Laboratory Performance Through Quality Contro...Randox
Randox Quality Control's latest educational guide examines Internal Quality Control, External Quality Assessment, Why laboratories should run QC, How often laboratories should run QC, Basic QC statistics and the quality control process.
Understanding statistics in laboratory quality controlRandox
This document discusses laboratory quality control and interpreting quality control results. It outlines a 5 step process: 1) Calculate the mean, 2) Calculate the standard deviation, 3) Establish decision limits, 4) Create a Levey-Jennings chart, and 5) Accept or reject results based on quality control rules. Statistics like the mean, standard deviation, and decision limits are used to monitor the accuracy and precision of analytical testing and ensure reliable patient results. Quality control software can automate the calculation of these statistics and generation of charts to more easily monitor performance.
The RX monaco is a fully automated clinical chemistry analyzer capable of performing 170 tests per hour. It has a discrete, random access design and features include a large test menu, quality control capabilities, intuitive Windows-based software, and remote diagnostics. The analyzer provides cost-effective and reliable testing for small to medium sized clinical laboratories.
The CBC machine is a common diagnostic tool used by doctors to measure a patient's red blood cell count, white blood cell count and platelet count. The machine uses a small sample of the patient's blood, which is then placed into special tubes and analyzed. The results of the analysis are then displayed on a screen for the doctor to review. The CBC machine is an important tool for diagnosing various conditions, such as anemia, infection and leukemia. It can also help to monitor a patient's response to treatment.
The document describes 6 models of the Stat Profile pHOx blood gas and critical care analyzer that provide different test menus and capabilities. The analyzers offer rapid turnaround times of 45-52 seconds and sample volumes as low as 45 microliters. Key features include an all-liquid calibration cartridge that eliminates gas tanks, automated on-board quality control, and connectivity to laboratory information systems. The analyzers provide physicians with comprehensive patient diagnostics using a compact point-of-care design.
The document describes the Applied Biosystems 7500 Fast and 7500 Real-Time PCR Systems. It summarizes the key features of the software, including options for high resolution melting analysis, gene expression studies, and melt curve analysis. It also outlines the performance specifications of the two systems, including sensitivity, dynamic range, run times, temperature accuracy, and dimensions. The 7500 Fast System is capable of completing runs in as little as 30 minutes while maintaining assay quality.
Olympus AU480 – An Ideal Choice for Low- to Mid-volume Laboratoriesblockscientific
A fully automated, random access chemistry system with STAT capability, the AU480 is a great choice for small to medium sized labs. Purchasing the Beckman Coulter Olympus AU480 chemistry analyzer from a reliable medical lab equipment dealer in New York would ensure great pricing. Established dealers offer refurbished models of this quality analyzer at great rates In addition to supplying necessary accessories, supplies and reagents, reliable suppliers also provide training and comprehensive maintenance support.
The document discusses PURELAB, a range of laboratory water purification systems from ELGA LabWater. PURELAB offers systems to produce different types (I-III) of purified water required for research applications. The systems use various technologies like ultrafiltration, UV treatment, and ion exchange to purify water. They are designed for reliability, ease of use, and to provide water of the necessary purity for different analytical techniques. The document provides details on several PURELAB models tailored for different throughput needs and feed water sources.
Biopharmaceutical manufacturing processes are complex, challenging and utilize living organisms to produce safe and efficacious biopharmaceuticals. These molecules themselves have high molecular weights and complex structures that will exhibit heterogeneity such that at any given vial contains not one active ingredient but a population of biologically active molecules which must have maximal benefit to the patient with minimal deleterious effects. The necessity for controlling variation in processes, and hence product, is self-evident when we consider how our actions affect the lives of the patients our products are developed for. This presentation focuses on understanding the various origins of process variation and examines strategies for reducing their impact or eliminating them all together.
http://parker.com/dh
توفر شركة تكنوسيرفيس مجموعة أجهزة الكشف عن المعادن Thermo Scientific ™ Sentinel ™ والتي تتميز بأداء كشف عالي الحساسية لجودة منتجك ومدي احتمالية العثور على ملوثات معادن حديدية وغير حديدية وأي ملوثات في الأطعمة والمشروبات وغيرها من المنتجات.
باستخدام تقنيات مبتكرة مثل Multiscan ™ و Selectscan ™ ، تساعد أجهزة الكشف عن المعادن Sentinel الشركات المصنعة على زيادة سلامة وصحة العملاء وتحسين جودة المنتج وزيادة كفاءة الإنتاج.
اكتشف معنا كيف يمكن لمجموعة منتجات Sentinel تلبية احتياجات تطبيقاتك.
أهمية وجود أجهزة الكشف المعادن في خط إنتاجك ؟
1️⃣ أصبح الآن من الشروط الأساسية لدي منظمة الصحة والأغذية لحمايه المستهلك.
2️⃣ ضروري لمنح شهادة الأيزو لمنتجك
3️⃣ ضمان استمرارية البراند الخاص بك في السوق وحصوله علي سمعة طيبة نتيجة ضمان الجودة
تستخدم هذه الاجهزه على خطوط انتاج وتعبئه الاغذيه
(مثل المطاحن و مصانع الالبان والحلويات والبسكويت والشيكولاته والمكرونه والمخللات والخضروات والفواكه المجمده والايس كريم ..وغيرها)
مميزات الجهاز:
◀يمكنه الكشف عن المعادن داخل منتجك خلال مراحل عمليه التصنيع حتى التعبئه وبدقه عاليه
◀ يمكنه رفض كل المنتجات المخالفه لمعايير الجوده وسلامه الغذاء
◀ يتميز الجهاز بالشكل الانسيابي وصغر الحجم
◀الجهاز حاصل على شهاده من هيئه سلامه الغذاء FDA
◀ الجهاز حاصل على IP69K لمقاومه الماء
◀ السير مصنوع من اعلى الخامات جوده والتي تتحمل الاوزان الكبيره
◀ سهل برمجته والتدريب عليه وتوافر قطع الغيار والصيانه
◀ ضمان لمده عام كامل
◀ الجهاز به إنذار صوت وضوء
◀ مهندسين متخصصين للتركيب والتدريب علي الجهاز وحاصلين علي شهادات معتمدة من ThermoFisher
تطبيقات اجهزه الكشف عن المعادن والشوائب :
تستهدف اجهزه الكشف عن المعادن والشوائب (metal detectors وال x-ray) كل شركات ومصانع الاغذيه وقطاع سلامه الغذاء وخطوط الانتاج التي تسعى للحصول على شهادات الايزو والجوده .
تسعى تكنوسيرفيس لخدمه جميع عملائها باحترافيه عن طريق مساعدتهم للوصول للنجاح في جميع المجالات السابقه .
just call us 01116593835
http://technoservice-egypt.com/
1) The document describes MEDICA water purification systems for clinical diagnostics. MEDICA systems provide consistent, high quality water to ensure accurate diagnostic test results from clinical analyzers.
2) Different MEDICA systems are suited for various applications depending on required water volumes and number of analyzers. The MEDICA-R and MEDICA-D systems provide 7-15 liters/hour of water for single analyzers, while the MEDICA Pro systems can supply up to 120 liters/hour to multiple large analyzers.
3) All MEDICA systems precisely control water quality through filtration, deionization, and UV treatment to achieve bacteria levels below standards and prevent interference in diagnostic tests.
Kemwell Biopharma provides analytical services including method development and validation, characterization, testing, and stability studies for biologics such as monoclonal antibodies. They have capabilities for chromatographic and electrophoretic methods as well as bioassays. Kemwell has experience conducting long-term stability studies from 2-36 months in various temperature conditions. Their facilities include analytical instrumentation, stability chambers, and data management systems to support GMP services. Kemwell offers various partnership models including fee-for-service, risk-sharing, and strategic long-term partnerships.
Life Cycle Management of Chromatographic Methods for BiopharmaceuticalsWaters Corporation
The development and manufacture of biopharmaceuticals is a dynamic and rapidly growing industry. By the nature of their production, biopharmaceuticals are highly complex heterogeneous mixtures that require many analytical techniques for characterization and routine testing. As a result, many manufacturers incorporate life cycle management into their respective workflows to take advantage of newer technologies and methodologies to ensure efficacy and patient safety.
In this presentation, we will address the range of chromatographic categories – HPLC, UHPLC, and UPLC – and define the characteristics associated with each. The discussion will continue with several examples of methods transferred from legacy HPLC instrumentation to modern UHPLC and UPLC instruments. We will compare qualitative and quantitative data across each chromatographic class. Resolution, sensitivity, and overall run time will be used as metrics to assess the success of the method transfer to the respective LC platform, to ensure the transferred methods are in line with current acceptance criteria.
Learn:
- The importance of selecting the correct instrumentation to meet user needs.
- Which parameters influence method transfer from one LC platform to another.
- How workflows can benefit from features such as Multi-flow path technology and Gradient SmartStart when transitioning methods.
Interested in more detail? Watch the related on-demand webinar: http://view6.workcast.net/register?pak=3479247014905635
This document provides information on laboratory equipment and services offered by a company. It describes their mission to distribute high-end laboratory solutions and support optimal laboratory operations. A variety of analytical instruments are highlighted, including those for organic synthesis, batch reactions, chromatography, sample preparation, elemental analysis, and more. The company aims to provide quality services like installations, training, maintenance, and technical support to customers.
For labs with complex challenges, there’s Altus™ UPLC® – the chromatography platform with best-in-class technology that’s already at work in labs the world over, delivering superior performance (with up to nine times the throughput of traditional
Today’s laboratories want more from their liquid chromatography system: Higher performance. Better reliability. More consistent and comprehensive analytical workflows. And most of all, more predictable and reproducible results. At the same time, you want
DCN Diagnostics offers OEM development services for complete lateral flow diagnostic systems. They have expertise in assay development, product engineering, manufacturing process development and commercialization assistance. Their services include reagent development, assay design, reader integration, design of plastic cassettes and cartridges, and manufacturing transfer. DCN has experience across various industries like medical diagnostics, veterinary, food testing, and can develop qualitative or quantitative lateral flow assays.
High-throughput and Automated Process Development for Accelerated Biotherapeu...KBI Biopharma
KBI Biopharma has developed high-throughput and automated processes to accelerate biotherapeutic development. This includes establishing a high-throughput process development team utilizing automated equipment and informatics solutions. Analytical case studies demonstrate automation of a residual host cell protein ELISA using a liquid handling robot, reducing analysis time from hours to minutes per sample. A second case study outlines development of a high-throughput size exclusion chromatography method, reducing run time from 30 minutes to 6 minutes while still effectively screening for high molecular weight species. These efforts allow for real-time data generation and monitoring of process development experiments.
Quality Control of RNA Samples - For Gene-Expression Results you Can Rely onQIAGEN
By their very nature RNA molecules, especially mRNA and regulator RNA, are labile and can be highly unstable and sensitive to heat, UV and RNase contamination. The quality, relevance and scientific impact of gene expression results directly depends on the ability to extract RNA without losing any fraction of interest, while preserving the integrity of the biological information it carries. RNA quality control is thus critical to ensure high-quality results and for turning these results into actionable insights with confidence.
In this webinar, we will introduce you to the main parameters influencing RNA-based assays and their respective impact on downstream applications, discuss how to monitor them and cover the advantages of automation for quality control along complex workflows.
The GeneDisc Rapid Microbiology System provides microbial test results in as little as two hours using quantitative PCR technology. The system consists of a DNA Extractor that prepares samples, GeneDisc plates that are loaded into a GeneDisc Cycler for analysis. It tests for key pathogens in biopharmaceuticals, foods, and water. The system offers simplicity, speed, security of results, and cost savings compared to traditional methods.
Similar to Acusera Verify Linearity Verification - June 17 LT674 (20)
This document provides a recipe for making pancakes, including a list of ingredients and instructions. It details the intended use as celebrating Lent, describes the recipe which supplies measurements for ingredients and instructions, and provides safety warnings about hot pans and overeating. Storage instructions note that pancakes should be eaten immediately. Limitations include others possibly eating the pancakes quickly and mixing up salt and sugar toppings. Materials required are listed but not provided. Quality control testing involves taste testing batches against standards and ensuring the control pancake is cooked correctly. Notes suggest kindness and recommend toppings.
The document appears to be a calendar listing return dates and deadlines for various quality control and proficiency testing programmes offered by RIQAS. It includes the programme codes, sample numbers, and return dates for each month of 2017. It also provides brief descriptions of new programmes being offered, such as a liquid CSF control with a 30-day open vial stability, a CYFRA 21-1 programme for immunoassay quality control, and programmes for PTH, immunosuppressant drugs, and sweat testing.
There are different types of QC material and each format will have it's own advantages & disadvantages. Each format will also need to be handled differently and this guide aims to explain the different methods for preparing each type of control.
ISO 15189 Accreditation Guide - Improving Laboratory Performance Through Qual...Randox
The document discusses ISO 15189 accreditation for medical laboratories. It outlines the importance of quality control and differences between accreditation and certification. Laboratories must implement both internal quality control and external quality assessment to gain ISO 15189 accreditation. This involves using third party controls, clinically relevant quality control material levels, peer group reporting, and participation in external quality assessment schemes. The document provides guidance on quality control considerations and processes needed to achieve and maintain ISO 15189 accreditation.
White Paper Quality Control for Point of Care TestingRandox
Point of care testing (POCT) refers to testing that is performed near or at the site of a patient with the result leading to a possible change in the care of the patient.
Multi-reglas de control de calidad (CC) son diseñadas y utilizadas para minimizar falsos rechazos y mantener una alta tasa de detección de errores. Hay seis reglas principales que son utilizadas para determinar si los resultados de una serie de muestras de pacientes deben ser aceptadas o rechazadas, basadas en el rendimiento de los materiales de control contra los criterios de las reglas. Diferentes combinaciones pueden ser aplicadas en función del número de controles, al error total permisible y al instrumento en uso. El siguiente diagrama de flujo se usa a menudo para determinar si una corrida debe ser aceptada o rechazada.
Troubleshooting QC Problems: Your QC has failed, what do you do next?Randox
Randox Quality Control's next 'Improving Laboratory Performance Through Quality Control' educational guide has been published with helpful tips that your laboratory can use in order to ensure it has effective troubleshooting procedures in place.
So you ran QC this morning and realised that one of your analytes has been flagged as 'out-of-control', what do you do next? Do you ignore the warning and continue patient testing, repeat the control until it's within range or do you halt patient testing and investigate the source of the error?
When it comes to troubleshooting QC errors, unfortunately there is no easy path to take. However, it's important that you have standard operating procedures in place, outlining what to do in the event of an out-of control error. Errors occur in laboratories all over the world. A lab with effective troubleshooting procedures in place will still have errors but will be able to detect them, quickly reducing their impact and reducing the risk of wasting both time and money.
About this webinar: This talk will introduce what cancer rehabilitation is, where it fits into the cancer trajectory, and who can benefit from it. In addition, the current landscape of cancer rehabilitation in Canada will be discussed and the need for advocacy to increase access to this essential component of cancer care.
DECODING THE RISKS - ALCOHOL, TOBACCO & DRUGS.pdfDr Rachana Gujar
Introduction: Substance use education is crucial due to its prevalence and societal impact.
Alcohol Use: Immediate and long-term risks include impaired judgment, health issues, and social consequences.
Tobacco Use: Immediate effects include increased heart rate, while long-term risks encompass cancer and heart disease.
Drug Use: Risks vary depending on the drug type, including health and psychological implications.
Prevention Strategies: Education, healthy coping mechanisms, community support, and policies are vital in preventing substance use.
Harm Reduction Strategies: Safe use practices, medication-assisted treatment, and naloxone availability aim to reduce harm.
Seeking Help for Addiction: Recognizing signs, available treatments, support systems, and resources are essential for recovery.
Personal Stories: Real stories of recovery emphasize hope and resilience.
Interactive Q&A: Engage the audience and encourage discussion.
Conclusion: Recap key points and emphasize the importance of awareness, prevention, and seeking help.
Resources: Provide contact information and links for further support.
Can coffee help me lose weight? Yes, 25,422 users in the USA use it for that ...nirahealhty
The South Beach Coffee Java Diet is a variation of the popular South Beach Diet, which was developed by cardiologist Dr. Arthur Agatston. The original South Beach Diet focuses on consuming lean proteins, healthy fats, and low-glycemic index carbohydrates. The South Beach Coffee Java Diet adds the element of coffee, specifically caffeine, to enhance weight loss and improve energy levels.
Chandrima Spa Ajman is one of the leading Massage Center in Ajman, which is open 24 hours exclusively for men. Being one of the most affordable Spa in Ajman, we offer Body to Body massage, Kerala Massage, Malayali Massage, Indian Massage, Pakistani Massage Russian massage, Thai massage, Swedish massage, Hot Stone Massage, Deep Tissue Massage, and many more. Indulge in the ultimate massage experience and book your appointment today. We are confident that you will leave our Massage spa feeling refreshed, rejuvenated, and ready to take on the world.
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Michigan HealthTech Market Map 2024. Includes 7 categories: Policy Makers, Academic Innovation Centers, Digital Health Providers, Healthcare Providers, Payers / Insurance, Device Companies, Life Science Companies, Innovation Accelerators. Developed by the Michigan-Israel Business Accelerator
Gemma Wean- Nutritional solution for Artemiasmuskaan0008
GEMMA Wean is a high end larval co-feeding and weaning diet aimed at Artemia optimisation and is fortified with a high level of proteins and phospholipids. GEMMA Wean provides the early weaned juveniles with dedicated fish nutrition and is an ideal follow on from GEMMA Micro or Artemia.
GEMMA Wean has an optimised nutritional balance and physical quality so that it flows more freely and spreads readily on the water surface. The balance of phospholipid classes to- gether with the production technology based on a low temperature extrusion process improve the physical aspect of the pellets while still retaining the high phospholipid content.
GEMMA Wean is available in 0.1mm, 0.2mm and 0.3mm. There is also a 0.5mm micro-pellet, GEMMA Wean Diamond, which covers the early nursery stage from post-weaning to pre-growing.
This particular slides consist of- what is Pneumothorax,what are it's causes and it's effect on body, risk factors, symptoms,complications, diagnosis and role of physiotherapy in it.
This slide is very helpful for physiotherapy students and also for other medical and healthcare students.
Here is a summary of Pneumothorax:
Pneumothorax, also known as a collapsed lung, is a condition that occurs when air leaks into the space between the lung and chest wall. This air buildup puts pressure on the lung, preventing it from expanding fully when you breathe. A pneumothorax can cause a complete or partial collapse of the lung.
At Apollo Hospital, Lucknow, U.P., we provide specialized care for children experiencing dehydration and other symptoms. We also offer NICU & PICU Ambulance Facility Services. Consult our expert today for the best pediatric emergency care.
For More Details:
Map: https://cutt.ly/BwCeflYo
Name: Apollo Hospital
Address: Singar Nagar, LDA Colony, Lucknow, Uttar Pradesh 226012
Phone: 08429021957
Opening Hours: 24X7
Healthy Eating Habits:
Understanding Nutrition Labels: Teaches how to read and interpret food labels, focusing on serving sizes, calorie intake, and nutrients to limit or include.
Tips for Healthy Eating: Offers practical advice such as incorporating a variety of foods, practicing moderation, staying hydrated, and eating mindfully.
Benefits of Regular Exercise:
Physical Benefits: Discusses how exercise aids in weight management, muscle and bone health, cardiovascular health, and flexibility.
Mental Benefits: Explains the psychological advantages, including stress reduction, improved mood, and better sleep.
Tips for Staying Active:
Encourages consistency, variety in exercises, setting realistic goals, and finding enjoyable activities to maintain motivation.
Maintaining a Balanced Lifestyle:
Integrating Nutrition and Exercise: Suggests meal planning and incorporating physical activity into daily routines.
Monitoring Progress: Recommends tracking food intake and exercise, regular health check-ups, and provides tips for achieving balance, such as getting sufficient sleep, managing stress, and staying socially active.
Letter to MREC - application to conduct studyAzreen Aj
Application to conduct study on research title 'Awareness and knowledge of oral cancer and precancer among dental outpatient in Klinik Pergigian Merlimau, Melaka'
The best massage spa Ajman is Chandrima Spa Ajman, which was founded in 2023 and is exclusively for men 24 hours a day. As of right now, our parent firm has been providing massage services to over 50,000+ clients in Ajman for the past 10 years. It has about 8+ branches. This demonstrates that Chandrima Spa Ajman is among the most reasonably priced spas in Ajman and the ideal place to unwind and rejuvenate. We provide a wide range of Spa massage treatments, including Indian, Pakistani, Kerala, Malayali, and body-to-body massages. Numerous massage techniques are available, including deep tissue, Swedish, Thai, Russian, and hot stone massages. Our massage therapists produce genuinely unique treatments that generate a revitalized sense of inner serenely by fusing modern techniques, the cleanest natural substances, and traditional holistic therapists.
2024 HIPAA Compliance Training Guide to the Compliance OfficersConference Panel
Join us for a comprehensive 90-minute lesson designed specifically for Compliance Officers and Practice/Business Managers. This 2024 HIPAA Training session will guide you through the critical steps needed to ensure your practice is fully prepared for upcoming audits. Key updates and significant changes under the Omnibus Rule will be covered, along with the latest applicable updates for 2024.
Key Areas Covered:
Texting and Email Communication: Understand the compliance requirements for electronic communication.
Encryption Standards: Learn what is necessary and what is overhyped.
Medical Messaging and Voice Data: Ensure secure handling of sensitive information.
IT Risk Factors: Identify and mitigate risks related to your IT infrastructure.
Why Attend:
Expert Instructor: Brian Tuttle, with over 20 years in Health IT and Compliance Consulting, brings invaluable experience and knowledge, including insights from over 1000 risk assessments and direct dealings with Office of Civil Rights HIPAA auditors.
Actionable Insights: Receive practical advice on preparing for audits and avoiding common mistakes.
Clarity on Compliance: Clear up misconceptions and understand the reality of HIPAA regulations.
Ensure your compliance strategy is up-to-date and effective. Enroll now and be prepared for the 2024 HIPAA audits.
Enroll Now to secure your spot in this crucial training session and ensure your HIPAA compliance is robust and audit-ready.
https://conferencepanel.com/conference/hipaa-training-for-the-compliance-officer-2024-updates
This particular slides consist of- what is hypotension,what are it's causes and it's effect on body, risk factors, symptoms,complications, diagnosis and role of physiotherapy in it.
This slide is very helpful for physiotherapy students and also for other medical and healthcare students.
Here is the summary of hypotension:
Hypotension, or low blood pressure, is when the pressure of blood circulating in the body is lower than normal or expected. It's only a problem if it negatively impacts the body and causes symptoms. Normal blood pressure is usually between 90/60 mmHg and 120/80 mmHg, but pressures below 90/60 are generally considered hypotensive.
2. Commercially Available GLU Method
Concentration (mg/dL)
Actual(mg/dL)
0 200 400 600 800
0
200
400
600
800
ACUSERA VERIFY
Keep your instrument in check with liquid
ready-to-use calibration verification materials
3. SOLUTIONS FOR ROCHE ANALYSERS
01
04
07
02
06
SOLUTIONS FOR BECKMAN ANALYSERS
DATA REDUCTION SOFTWARE
INDEX
BENEFITS
08 RELATED PRODUCTS
11 RANDOX - A GLOBAL DIAGNOSTIC SOLUTIONS PROVIDER
12 CONTACT US
4. Our range of instrument dedicated, liquid ready-to-use calibration verifiers is designed to challenge
the entire Analytical Measuring Range, whilst helping to meet CLIA requirements and remaining
convenient to use.
Liquid ready-to-use
•All samples are provided in a user-friendly,liquid ready-to-use format significantly reducing preparation
time and the risk of pipetting errors.
Clinically relevant levels
• Specifically designed to challenge the complete Analytical Measuring Range (AMR),helping to ensure
accurate and reliable instrument performance.A minimum of 5 levels eliminates the need for manual
dilution and allows for more comprehensive assessment than the minimum requirement of 3 levels
set by CLIA.
Instrument Dedicated
• Help to ensure specific instrument requirements are met with the availability of dedicated solutions
for both Beckman and Roche Cobas systems.
Stability
• An extended open vial stability keeps waste to a minimum and ensures availability of product for
troubleshooting.
Data Reduction Software
• Complimentary data reduction software is provided delivering an immediate indication of performance.
BENEFITS
1
Consolidation
• Reduce costs,storage space and the number of individual products required to cover your test menu with
our comprehensive, multi-analyte CalibrationVerifiers.
5. SOLUTIONS FOR BECKMAN ANALYSERS
2
Description Size Cat. No.
Cardiac LinearityVerifiers (for Beckman systems) 5 x 2 ml LV10151
Analytes
CK-MB Mass | Myoglobin | Troponin I
Cardiac Markers
Comprising three common cardiac markers in a liquid
ready-to-use format, the Acusera cardiac linearity
material is designed to objectively verify calibration
whilst remaining convenient and easy to use. Five
distinct levels are provided, spanning the instruments’
reportable range.
Benefits
• Convenient, liquid ready-to-use format
• 5 levels provided
• 30 day open vial stability at 2ºC to 8ºC
• Shelf life up to 2 years from date of manufacture
Description Size Cat. No.
Protein 1 LinearityVerifiers (for Beckman AU systems) 5 x 1.5 ml LV10147
Analytes
ASO | Complement C3 | Complement C4 | CRP | Ferritin | IgA | IgG | IgM | Prealbumin | Transferrin
Specific Proteins 1
Uniquely combining ten serum proteins, reducing the
number of individual products required to cover your
test menu. Designed primarily for use with Beckman
AU systems, specific instrument requirements are
met. Five distinct levels are provided in a user-friendly
liquid ready-to-use format.
Benefits
• Convenient, liquid ready-to-use format
• 5 levels provided
• 30 day open vial stability at 2ºC to 8ºC
• Shelf life up to 3 years from date of manufacture
Description Size Cat. No.
Protein 2 LinearityVerifiers (for Beckman AU systems) 5 x 1.5 ml LV10148
Analytes
α-1-Acid-Glycoprotein | α-1-Antitrypsin | β-2 Microglobulin | Ceruloplasmin | Haptoglobin
Specific Proteins 2
Designed to effectively challenge the instruments’
reportable range, the Acusera Specific Proteins 2
linearity material comprises five common serum
proteins. Five distinct levels are supplied in a
convenient liquid ready-to-use format with assayed
values available for Beckman AU systems.
Benefits
• Convenient, liquid ready-to-use format
• 5 levels provided
• 30 day open vial stability at 2ºC to 8ºC
• Shelf life up to 3 years from date of manufacture
6. SOLUTIONS FOR BECKMAN ANALYSERS
3
Description Size Cat. No.
Therapeutic Drug Monitoring LinearityVerifiers (for Beckman systems) 5 x 3 ml LV10149
Analytes
Acetaminophen | Amikacin | Caffeine | Carbamazepine | Digoxin | Disopyramide | Ethosuximide | Gentamicin
Lidocaine | Lithium | N-Acetylprocainamide | Phenobarbital | Phenytoin | Primidone | Procainamide | Quinidine
Salicylate | Theophylline | Tobramycin | Valproic Acid | Vancomycin
Therapeutic Drugs
Specifically designed for use with Beckman AU
systems, five unique levels are supplied spanning
the instruments’ reportable range. A total of 21
therapeutic drugs are presented in a single, liquid
ready-to-use product eliminating the need to
purchase additional material to cover your test menu
while remaining easy and convenient to use.
Benefits
• Convenient, liquid ready-to-use format
• 5 levels provided
• 14 day open vial stability at 2ºC to 8ºC
• Shelf life up to 3 years from date of manufacture
In order to ensure the highest possible standards in laboratory testing, CLIA
has recommended that laboratories perform and document calibration
verification procedures at least twice per year and/or in the event of the
following;
Change of reagents | Instrument maintenance | Poor QC results | New instrument
7. 4
SOLUTIONS FOR ROCHE ANALYSERS
Description Size Cat. No.
Cardiac LinearityVerifiers (for Roche Cobas systems) 6 x 2 ml LV10150
Analytes
CK-MB Mass | D-Dimer | Myoglobin | NT-proBNP | TroponinT | hsTroponinT
Cardiac Markers
Uniquely combining six common cardiac markers in a
user friendly, liquid ready-to-use format, preparation
time is significantly reduced. Designed for use with
Roche Cobas systems, six unique levels are supplied
ensuring accurate assessment of the instruments
reportable range.
Benefits
• Convenient, liquid ready-to-use format
• 6 levels provided
• 30 day open vial stability at 2ºC to 8ºC
• Shelf life up to 2 years from date of manufacture
Description Size Cat. No.
Protein 1 LinearityVerifiers (for Roche Cobas systems) 6 x 1 ml LV10143
Analytes
Complement C3 | Complement C4 | IgA | IgG | IgM | Transferrin
Specific Proteins 1
Uniquely combining six serum proteins, reducing the
number of individual products required to cover your
test menu. Designed primarily for use with Roche
Cobas systems, specific instrument requirements are
met. Five distinct levels are provided in a user-friendly
liquid ready-to-use format.
Benefits
• Convenient, liquid ready-to-use format
• 5 levels provided (6 for IgA, IgG and IgM)
• 30 day open vial stability at 2ºC to 8ºC
• Shelf life up to 3 years from date of manufacture
Description Size Cat. No.
Protein 2 LinearityVerifiers (for Roche Cobas systems) 5 x 1 ml LV10144
Analytes
α-1-Acid Glycoprotein | α-1-Acid Antitrypsin | β-2-Microglobulin | Ceruloplasmin
Specific Proteins 2
Designed to effectively challenge the instruments’
reportable range, five distinct levels are supplied in
a convenient liquid ready-to-use format with assayed
values available for Roche Cobas systems.
Benefits
• Convenient, liquid ready-to-use format
• 5 levels provided
• 30 day open vial stability at 2ºC to 8ºC
• Shelf life up to 3 years from date of manufacture
8. 5
SOLUTIONS FOR ROCHE ANALYSERS
Description Size Cat. No.
Protein 3 LinearityVerifiers (for Roche Cobas systems) 6 x 1 ml LV10145
Analytes
ASO | CRP | Haptoglobin
Specific Proteins 3
Comprising three serum proteins, theAcusera Specific
Proteins 3 linearity material is designed to effectively
challenge the instruments’ reportable range, six
distinct levels are supplied in a convenient liquid
ready-to-use format with assayed values available for
Roche Cobas systems.
Benefits
• Convenient, liquid ready-to-use format
• 6 levels provided (5 for Haptoglobin)
• 30 day open vial stability at 2ºC to 8ºC
• Shelf life up to 3 years from date of manufacture
Description Size Cat. No.
Protein 4 LinearityVerifiers (for Roche Cobas systems) 6 x 1 ml LV10146
Analytes
Albumin | Prealbumin | Rheumatoid Factor
Specific Proteins 4
Comprising three serum proteins, theAcusera Specific
Proteins 4 linearity material is designed to effectively
challenge the instruments’ reportable range while
remaining easy and convenient to use. Six distinct
levels are supplied with assayed values available for
Roche Cobas systems.
Benefits
• Convenient, liquid ready-to-use format
• 6 levels provided (5 for Rheumatoid Factor)
• 30 day open vial stability at 2ºC to 8ºC
• Shelf life up to 3 years from date of manufacture
9. 6
DATA REDUCTION SOFTWARE
Complimentary data reduction software is available for use with all Randox calibration verification
sets, delivering instant access to a wide range of functionality to make the data review process faster.
• Cloud based software allowing convenient access from anywhere in the lab
• Intuitive user-friendly interface with simple data entry functionality
• Easy-to-interpret,interactive charts for at-a-glance performance assessment
• Unique traffic light system indicating pass or fail
• Automatically generated statistics
• Peer group data updated live in real-time for faster troubleshooting
Providing instant access to automatically generated charts,
statistics and real-time peer group data, the Acusera Verify
software is designed to significantly reduce the time spent
analysing data, facilitating immediate laboratory decisions.
Did you know you can manage both daily QC activities and calibration verification on one centralised
platform? Find out more at www.randoxqc.com
10. INDEX
7
Cardiac Markers Beckman Access Roche Cobas
CK-MB Mass
D-Dimer -
Myoglobin
NT-proBNP -
Troponin I -
Troponin T -
hsTroponin T -
Specific Proteins 1 Beckman AU Roche Cobas
ASO -
Complement C3
Complement C4
CRP -
Ferritin -
IgA
IgG
IgM
Prealbumin -
Transferrin
Specific Proteins 2 Beckman AU Roche Cobas
a-1-Acid Glycoprotein
a-1-Antitrypsin
b-2-Microglobulin
Ceruloplasmin
Haptoglobin -
Specific Proteins 3 Beckman AU Roche Cobas
ASO -
CRP -
Haptoglobin -
Specific Proteins 4 Beckman AU Roche Cobas
Albumin -
Prealbumin -
Rheumatoid Factor -
TDM Beckman AU Roche Cobas
Acetaminophen -
Amikacin -
Caffeine -
Carbamazepine -
Digoxin -
Disopyramide -
Ethosuximide -
Gentamicin -
Lidocaine -
Lithium -
N-Acetylprocainamide -
Phenobarbital -
Phenytoin -
Primidone -
Procainamide -
Quinidine -
Salicylate -
Theophylline -
Tobramycin -
Valproic Acid -
Vancomycin -
Dedicated solutions are available for Roche Cobas Beckman systems. Use the table below to
determine the best solution for your lab.
11. 8
RELATED PRODUCTS
As a world leading manufacturer of multi-analyte true third party controls, thousands of laboratories rely on Randox to
accurately assess test system performance and ultimately empower them with the confidence required to release patient
test results. With more than 390 analytes available, the number of individual controls required to cover your test menu is
significantly reduced while simultaneously reducing costs, time and storage space. A choice of formats is available, including
liquid or lyophilised, which ensures flexibility and suitability for laboratories of all sizes and budgets. Helping you to meet
ISO 15189:2012 requirements:
• Designed to react to the test system in the same manner as a patient sample, helping to reduce inconvenient shifts in QC
results when reagent batch is changed and ultimately providing a true indication of laboratory performance.
• The presence of analytes at key decision levels ensures accurate instrument performance and eliminates the need for
additional low/high controls at extra expense.
• Manufactured independently from any instrument, the Acusera range delivers unbiased performance assessment with any
instrument or method, while eliminating the need for multiple instrument specific controls.
Product Portfolio
Antioxidants | Blood Gas | Cardiac Markers | Routine Chemistry | Coagulation | Haematology | Diabetes
Immunoassay | Immunology | Lipids | POCT | Therapeutic Drugs | Toxicology | Urine Chemistry
True third party quality controlsACUSERA
Uniquely combining more than 100 analytes conveniently in a single
control, laboratories can significantly reduce costs and consolidate
without compromising on quality. As true third party controls, unbiased
performance assessment with any instrument or method is guaranteed.
12. Interlaboratory Data ManagementACUSERA 24•7
Designed for use with the Acusera range of third party controls, the Acusera 24•7 software helps laboratories monitor and
interpret their QC data. Access to an impressive range of features, including interactive charts, the automatic calculation of
Measurement Uncertainty Sigma Metrics and live peer group data generated from our extensive database of laboratory
participants, ensures Acusera 24•7 is the most comprehensive package available.
• Advanced statistical analysis with automatic calculation of performance metrics including; Sigma, UM,TE %Bias.
• Instantly discover how you compare to your peers with peer group statistics updated live in real-time reducing time and
money spent troubleshooting.
• Interactive charts allowing you to add events and multiple data sets for quick and easy performance monitoring.
• Automated data import with bi-directional connection to LIMS (eliminating manual data entry).
Software Features
Dashboard | Result History | Interactive Levey-Jennings Charts | Interactive Histogram Charts
Performance Summary Charts | Statistical Analysis Report | Statistical Metrics Report
Uncertainty of Measurement Report | Exception Report | Peer Group Statistics | Acusera Advisor
Audit Trail Report
‘The laboratory shall have a procedure to prevent the release of patient
results in the event of quality control failure. When the quality controls
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
RELATED PRODUCTS
9
13. 10
Boasting over 45,000 participants and more than 360 parameters across 32 comprehensive flexible EQA programmes,
RIQAS is the largest international EQA scheme. Designed to cover all areas of clinical testing, each of our multi-analyte
programmes is designed to reduce the number of individual programmes required saving precious laboratory time and
money. In addition each programme benefits from a wide range of concentrations, frequent reporting, rapid feedback and
informative yet user-friendly reports.
• Programmes accredited to ISO/IEC 17043 helping laboratories to meet ISO 15189:2012 requirements.
• Simple one page per parameter report format enables at-a-glance performance assessment saving time spent analysing
results.
• Rapid report turnaround within 72 hours from the submission deadline ensures any corrective actions can be taken
quickly, minimising the number of sample repeats required.
• Laboratories can register up to 5 instruments per programme at no extra cost and receive a complimentary multi-
instrument report for comparative performance assessment.
Programme Offering
Ammonia/Ethanol | Anti-TSH Receptor | Blood Gas | BNP | Cardiac | Cerebrospinal Fluid (CSF) | Clinical Chemistry
Coagulation | CYFRA 21-1 | ESR | Glycated Haemoglobin (HbA1c) | Haematology | Human Urine
Immunoassay | Immunoassay Speciality 1 | Immunoassay Speciality 2 | Immunosuppressant | Lipid | Liquid Cardiac
Maternal Screening | Serology (EBV) | Serology (HIV/Hepatitis) | Serology (Syphilis) | Serology (ToRCH)
Specific Proteins | Sweat Testing | TDMs | Trace Elements in Blood | Trace Elements in Serum
Trace Elements in Urine | Urinalysis | Urine Toxicology
Randox International Quality Assessment SchemeRIQAS
RELATED PRODUCTS
With over 45,000 lab participants, peer group numbers are maximised
ensuring availability of data for a wide range of instruments and methods.
14. RANDOX - A GLOBAL DIAGNOSTIC SOLUTIONS PROVIDER
RX series of Clinical Analysers
The RX series combines robust hardware and intuitive software with the world leading RX series test menu, including
routine chemistries, specific proteins, lipids, therapeutic drugs, drugs of abuse, antioxidants and diabetes testing. Renowned
for quality and reliability, the RX series boasts one of the most extensive dedicated clinical chemistry test menus on the
market guaranteeing real cost savings through consolidation of routine and specialised tests onto a single platform. This
extensive dedicated test menu of high quality reagents guarantees excellence in patient care reducing costly test re-runs
or misdiagnosis and offers unrivalled precision and accuracy for results you can trust.
Biochemistry Reagents
Randox offers an extensive range of diagnostic reagents, giving biochemistry laboratories the opportunity to advance their
routine and niche testing.The Randox reagents range goes beyond routine chemistries. At Randox we re-invest significantly
in research and development to ensure we meet the ever changing needs of the laboratory. As a result, the esoteric
reagents range from Randox is extensive and includes sLDL, Lipoprotein(a), H-FABP, Cystatin C, TxBCardio, Adiponectin,
Bile Acids, Copper, D-3-Hydroxybutyrate, G-6-PDH, Non-Esterified Fatty Acids,Total Antioxidant Status and Zinc. Randox
Reagents provide a number of benefits for the laboratory: Cost savings through excellent stability, automated methods
and standards supplied with some kits; confidence in results with high performance methods, minimal interferences and
wide measuring ranges; convenience and choice with applications for over 100 biochemistry analysers; liquid ready-to-use
reagents, a wide range of kit sizes and complementary controls and calibrators.
Biochip Array Technology
Biochip ArrayTechnology (BAT) is an innovative assay technology for multi-analyte screening of biological samples in a rapid,accurate
and easy to use format. BAT offers highly specific tests, coupled to highly sensitive chemiluminescent detection, providing quantitative
results in easy to interpret reports. Randox BAT assays offer diagnostic, prognostic and predictive solutions across a variety of
disease areas including sexually transmitted infection, cardiovascular disease (CVD), familial hypercholesterolemia (FH), colorectal
cancer and respiratory infection.
Randox has been supplying laboratories worldwide with revolutionary
diagnostic solutions for over 30 years. Our experience and expertise
allow us to create a leading product portfolio of high quality diagnostic
tools which offer reliable and rapid diagnosis. We believe that by providing
laboratories with the right tools, we can improve healthcare worldwide.
11
15. 12
CONTACT US
For technical support contact:
technical.services@randox.com
Head Quarters
Randox Laboratories Ltd, 55 Diamond Road, Crumlin, County Antrim, BT29 4QY, United Kingdom
+44 (0) 28 9442 2413 marketing@randox.com randoxqc.com
Contact us for more information on any of our products and services:
PORTUGAL
Irlandox Laboratorios Quimica Analitica Ltda
Tel: +351 22 589 8320
PUERTO RICO
Clinical Diagnostics of Puerto Rico, LLC
Tel: +1 787 701 7000
POLAND
Randox Laboratories Polska Sp. z o.o.
Tel: +48 22 862 1080
ITALY
Randox Laboratories Ltd.
Tel: +39 06 9896 8954
INDIA
Randox Laboratories India Pvt Ltd.
Tel: +91 80 2802 5000
HONG KONG
Randox Laboratories Hong Kong Limited
Tel: +852 3595 0515
SLOVAKIA
Randox S.R.O.
Tel: +421 2 6381 3324
SOUTH AFRICA
Randox Laboratories SA (Pty) Ltd.
Tel: +27 (0) 11 312 3590
REPUBLIC OF IRELAND
RandoxTeoranta
Tel: +353 7495 22600
FRANCE
Laboratoires Randox
Tel: +33 (0) 130 18 96 80
GERMANY
Randox Laboratories GmbH
Tel: +49 (0) 215 1937 0611
CZECH REPUBLIC
Randox Laboratories S.R.O.
Tel: +420 2 1115 1661
SPAIN
Laboratorios Randox S.L.
Tel: +34 93 475 09 64
SWITZERLAND
Randox Laboratories Ltd. (Switzerland)
Tel: +41 41 810 48 89
SOUTH KOREA
Randox Korea
Tel: +82 (0) 31 478 3121
USA
Randox Laboratories-US, Ltd.
Tel: +1 304 728 2890
VIETNAM
Randox Laboratories Ltd.Vietnam
Tel: +84 (0) 8 3911 0904
UAE
Randox Medical EquipmentsTrading LLC
Tel: +971 55 474 9075
BRAZIL
Randox Brasil Ltda.
Tel: +55 11 5181-2024
CHINA
Randox Laboratories Ltd.
Tel: +86 021 6288 6240
AUSTRALIA
Randox (Australia) Pty Ltd.
Tel: +61 (0) 2 9615 4640
International Offices
16. LT674JUN17
Information correct at time of print.Randox Laboratories Ltd is a subsidiary of Randox Holdings Limited a company registered within Northern Ireland with company number N.I.614690. VAT Registered Number:GB 151
6827 08.Product availability may vary from country to country.Please contact your local Randox representative for information.Products may be for Research Use Only and not for use in diagnostic procedures in the USA.