July 2020 - July 2021

A Bio-Rad Quality Control Virtual Conference

Powering Exceptional Labs

We are pleased to announce the Bio-Rad Quality Control Virtual Conference 2020. This online event brings together Clinical Laboratory Professionals from around the world to discover the latest innovative QC products and data management solutions, with access to new monthly webinars designed to help laboratorians raise the bar in their QC practice. More laboratories trust Bio-Rad for independent quality control products than any other manufacturer.

Join the Quality Control Virtual Conference to:

Attend live webinars or view on-demand educational webinars covering a variety of important QC topics and earn free P.A.C.E. CE credits by joining any of the webinars
Access and download a selection of scientific posters
Visit product booths to learn more information about featured products, view videos, download brochures, infographics and other literature

This free online conference will remain open around the clock with webinars broadcast throughout 2020, so check back frequently for new information.

Speakers

Curtis Parvin, PhD

Biostatistical Advisor
Duane W. Newton, PhD, D(ABMM), FIDSA

Director, Clinical Microbiology Laboratory, Associate Director, Division of Clinical Pathology, Professor of Pathology, University of Michigan
Elitza S. Theel, PhD, D(ABMM)

Director, Infectious Diseases Serology Laboratory, Clinical Microbiology Division, Department of Laboratory Medicine and Pathology, the Mayo Clinic, Minnesota
John Yundt-Pacheco, MSCS

Scientific Fellow, Bio-Rad Laboratories

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NOV 12, 2020 6:00 AM PST

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SEP 10, 2020 9:30 AM EDT

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Agenda

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AUG 26, 2020 11:00 AM PDT | AUGUST 27, 11:00 AM SGT | AUGUST 27, 4:00 PM CEST
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SARS-CoV-2 Quality Control for Molecular and Serology assays

SARS-CoV-2 has created significant challenges for laboratories, requiring the development, validation, and scale up of testing in a very short time period--often this was done for multiple methods due to capacity demands and supply chain shortages. Part of assuring quality test results is the confidence in testing that comes from a robust QC Program. In this webinar, the speakers will discuss different issues to be considered for QC material selection, as well as QC program design & strategies for SARS-CoV-2 molecular and serology testing.

Learning Objectives:

1. Describe approaches to quality control for SARS-CoV-2 molecular testing that monitor the entire testing process

2. Discuss quality control approaches for high-throughput SARS-CoV-2 antibody tests

3. List 2 optimal QC practices for each methodology

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Duane W. Newton, PhD, D(ABMM), FIDSA
Director, Clinical Microbiology Laboratory, Associate D...

Elitza S. Theel, PhD, D(ABMM)
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SEP 16, 2020 11:00 AM | SEPT 17, 11:00 AM SGT | SEPT 17, 4:00 PM CEST
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How to Limit Patient Harm from Erroneous Results, QC Strategies Based on Risk Management

John Yundt-Pacheco, MSCS

Scientific Fellow, Bio-Rad Laboratories

Quality Control design has for many years been focused around instrument performance. But with the new risk management approaches emerging the focus is now moving to the risk of erroneous results for patients. This presentation will describe this new approach designed to prevent patient harm from erroneous results to acceptable levels.

Learning Objectives:
1. Identify the steps in patient risk managed QC strategy design.
2. Explain how to set the Severity of Harm category for an analyte.
3. Describe 2 components of the QC design that can be changed to minimize patient risk.

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JUL 15, 2020 11:00 AM PDT

Best Practices in Quality Control: 10 Simple Recommendations

Curtis Parvin, PhD

Biostatistical Advisor

Designing a good QC plan can be a daunting task. These simple recommendations can provide guidance to the lab and are essential to include in a good QC plan. They have been used and proven effective by many labs.

Learning Objectives:

1. Identify factors in QC error that contribute to increased patient risk.

2. Describe ways in which quality risk management has contributed to an added set of values that the laboratory should be aware of.

3. Recommend 5 QC practices which you can apply in your lab.

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Speakers

Curtis Parvin, PhD
Biostatistical Advisor

Biography
Dr. Parvin served 30 years on the faculty of Washington University School of Medicine as Director of Informatics and Statistics in the Division of Laboratory and Genomic Medicine. Dr. Parvin's training is in biostatistics and medical informatics and focused his career on the application of statistical theory to problems relevant to laboratory medicine. He has co-authored numerous papers that have published in the leading laboratory medicine journals. Dr. Parvin joined Bio-Rad in 2009 as Manager of Advanced Statistical Research in Bio-Rad's Quality Systems Division. He recently entered semi-retirement. He still enjoys working with labs that are looking to improve their QC design and presenting at laboratory conferences around the world.
Duane W. Newton, PhD, D(ABMM), FIDSA
Director, Clinical Microbiology Laboratory, Associate Director, Division of Clinical Pathology, Professor of Pathology, University of Michigan

Biography
Duane Newton, Ph.D., D(ABMM) is currently the Director of the Clinical Microbiology Laboratory, as well as the Associate Director of the Division of Clinical Pathology, both in the Department of Pathology at Michigan Medicine. Dr. Newton completed Post-Doctoral training at the University of Tennessee and the VA Medical Center in Memphis, Tennessee and a Clinical and Public Health Microbiology Fellowship at the University of Rochester Medical Center, Clinical Microbiology Laboratories in Rochester, New York. In 2000 he was appointed as Manager of the Virology/Immunology Section of the Department of Community Health, Division of Infectious Diseases, Bureau of Laboratories for the State of Michigan and as Adjunct Assistant Professor for the Michigan State University Medical Technology Program. In 2002, he joined the faculty of the Department of Pathology at the University of Michigan Medical School as Clinical Assistant Professor and Associate Director of the Microbiology/Virology Laboratories. Dr. Newton was named Director of Microbiology/Virology Laboratories in 2003 and received his certification as a Diplomate by the American Board of Medical Microbiology in 2004. His research interests lie in the development of molecular assays for the diagnosis and management of infectious diseases.
Elitza S. Theel, PhD, D(ABMM)
Director, Infectious Diseases Serology Laboratory, Clinical Microbiology Division, Department of Laboratory Medicine and Pathology, the Mayo Clinic, Minnesota

Biography
Elitza S. Theel, Ph.D., D(ABMM), is the Director of the Infectious Diseases Serology Laboratory at Mayo Clinic and an Associate Professor of Laboratory Medicine And Pathology at the Mayo Clinic College of Medicine in Rochester, Minnesota. Dr. Theel completed her Postdoctoral Fellowship in Clinical and Public Health Microbiology at the Mayo School of Graduate Medical Education after she graduated with her PhD in Medical Microbiology and Immunology from the University of Wisconsin-Madison. Her interests include development and evaluation of serologic methods, including antibody and antigen detection assays, for diagnosis of difficult to culture or otherwise identify infectious diseases. Dr. Theel has evaluated over 15 different serologic tests for detection of antibodies to SARS-CoV-2 over the past few months and has co-development a neutralizing antibody test for the virus, which is currently being used to screen potential plasma donors as part of the national COVID-19 convalescent plasma clinical trials.
John Yundt-Pacheco, MSCS
Scientific Fellow, Bio-Rad Laboratories

Biography
Mr. Yundt-Pacheco performs research in quality control and patient risk issues in the Informatics Discovery Group at Bio-Rad. John has had the opportunity to work with laboratories around the world, developing practical real time, inter-laboratory quality control and proficiency testing systems. As an innovator, has developed numerous ideas leading to 37 laboratory related invention patents around the globe. John holds a Master's degree in Computer Science from University of Texas at Dallas with a focus on Intelligent Systems and has a Post Master's Certificate in Sequence Analysis and Genomics, and is a degree candidate for a Master's degree in Biotechnology at Johns Hopkins University. In addition to authoring articles and papers on QC design, he is a popular speaker on laboratory QC and QA topics at international conferences.

C.E. Credits

The speakers below have been approved for Continuing Education Credits. To redeem your credits, locate the presentation you watched and click on the CE buttons for further direction. For more general information regarding continuing education, the processes to receive credits, and the accreditation bodies, Click here

JUL 15, 2020 11:00 AM PDT

Best Practices in Quality Control: 10 Simple Recommendations

Curtis Parvin, PhD

Biostatistical Advisor

Presented at: A Bio-Rad Quality Control Virtual Conference

Florida CE

P.A.C.E. CE
AUG 26, 2020 11:00 AM PDT | AUGUST 27, 11:00 AM SGT | AUGUST 27, 4:00 PM CEST
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SARS-CoV-2 Quality Control for Molecular and Serology...

Presented at: A Bio-Rad Quality Control Virtual Conference

Florida CE

P.A.C.E. CE
SEP 16, 2020 11:00 AM | SEPT 17, 11:00 AM SGT | SEPT 17, 4:00 PM CEST
Add to Calendar Select one of the following: iCal Google Calendar Outlook Calendar Yahoo Calendar

How to Limit Patient Harm from Erroneous Results, QC...

John Yundt-Pacheco, MSCS

Scientific Fellow, Bio-Rad Laboratories

Presented at: A Bio-Rad Quality Control Virtual Conference

Florida CE

P.A.C.E. CE

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