Featured Webinar

Our three Summer School sessions comprise of on-demand webinars and supporting white papers, to help deepen your understanding of quality control practices in the clinical laboratory. Summer School has started... enjoy!

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During this webinar, Oswald will present a comprehensive approach

to QC processes that integrates the principles of efficiency, costeffectiveness,

and sustainability.

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This webinar explains how to identify problems and errors in the analytical process, and be shown how quality control material is a very helpful tool. You’ll also learn what steps are needed to make corrections and how to avoid reporting erroneous patient results, which will ultimately contribute to the welfare of patients.

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This webinar explains the basic steps on how to proceed with quality control procedures in the daily routine. You will learn when and how quality control material should be used. What is the outcome of the measurement of a quality control product and what needs to be done if results are outside the limits.

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Learn about the latest developments in the standard ISO 15189:2022 “Medical laboratories - Requirements for quality and competence”. It has been developed with the objective of promoting the welfare of patients through confidence in the quality and competence of medical laboratories.

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A panel of industry experts discussed global QC practice and future trends and developments.

This event took place on Tuesday, July 26 | 7:00AM - 8:30AM Marriott Marquis, Grand Lakes Ballroom A, Chicago IL.

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Through this webinar the participant will learn about the latest developments in the standard ISO/IEC 17025:2017 “General requirements for the competence of testing and calibration laboratories”. It has been developed with the objective of promoting the welfare of patients through confidence in the quality and competence of medical laboratories.

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Technopath are proud to sponsor this free educational webinar, delivered by our very own Ger Kennedy and hosted by Select Science. LEARN MORE

Estimates of analytical, within-subject, and between-subject biological variation are extremely important for the interpretation of test results. The data is usually generated by prospective studies. An EFLM Task Group has developed an evidence based database containing data on biological variation as well as estimates of analytical performance specifications and reference change values. LEARN MORE

The concept of traceability in laboratory medicine usually concerns the analytical phase. In particular, traceability to a common reference, ideally up to the International System of Units [SI], ensures high quality and long-term equivalence of measurement results obtained by different measuring systems.

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Despite monumental advances in quality improvement over the past few decades, clinical laboratories are still under increasing pressure to achieve efficiency, timeliness, safety, effectiveness and patient-centered services. LEARN MORE

Learn about generating QC reports in IAMQC®, including Six Sigma, MU, and Reagent Tracking. Learn more here.

Quality controls are a helpful tool in method comparisons. Learn more here.

Internal quality controls play a key role in quality assurance of laboratory examinations. Learn more here.

Join us for a webinar to recalibrate your thinking on QC rules and runs, perhaps something you haven't done in like 10, 20, 30 years?!?! Watch on-demand here.

In March 1981, the "Westgard Rules" were born. Join us for a discussion of the past, present, and future of multirule QC.

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This presentation will describe the differences between clinical chemistry testing and infectious disease serology. By understanding these differences, laboratory staff can better understand the causes of variation in the test system.

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Qualitative examinations are those that measure the presence or absence of a substance. The results are not expressed in numerical terms, but in descriptive or qualitative terms such as “positive,” “negative,” “reactive,” “non-reactive,” “normal,” or “abnormal”. We will consider how Internal Quality Control is applied in this context.

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Join us for a webinar to learn about quality control (QC) regulations, setting the proper QC strategy/design, and troubleshoot SARualitative tests in the laboratory.

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In this lecture, Sten Westgard revisits “the argument and established rationale for Liquid Controls vs Lyophilised Controls, Linearities and figuring out the reportable range and more..

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Measurement Uncertainty is a key element in laboratory medicine. We have learned to monitor quality of laboratory results using internal and external quality controls.

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This one hour zoom with Professor Sten Westgard will introduce the concepts of Six Sigma, Sigma Metrics, and Westgard Sigma Rules.

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This webinar will give an overview on the changes and challenges derived from the IVDR with a special focus on medical laboratories.

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Der Vorstand der Bundesärztekammer hat der überarbeiteten Version der Richtlinie zur Qualitätssicherung laboratoriumsmedizinischer Untersuchungen (Rili-BÄK) im Oktober 2019 zugestimmt. In der neuen Fassung wurden u. a. Weiterentwicklungen im Bereich des Qualitätsmanagements übernommen, neue Messgrößen aufgenommen und die Vorgaben für die Messgröße HbA1c angepasst

Weitere Informationen finden Sie hier

Watch this webinar to see Wayne Dimech and Sten Westgard assess the landscape for COVID-19 testing, consider the current methods, tests, protocols and the state of regulations.

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