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Agenda
  • Practical Tips to Manage Laboratory QC Data
    MAY 19, 2021 8:00 AM PDT
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    Practical Tips to Manage Laboratory QC Data
    James H. Nichols, Ph.D., DABCC, FAACC
    Professor of Pathology, Microbiology, and Immunology, Medical Director of Clinical Chemistry and Point-of-Care Testing at Vanderbilt University School of Medicine
  • The Diagnostic & Clinical Impact of SARS-CoV-2 Variants
    MAY 26, 2021 8:00 AM PDT
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    The Diagnostic & Clinical Impact of SARS-CoV-2 Variants
    Adam Lauring, MD, PhD
    Associate Professor in the Department of Internal Medicine/Division of Infectious Diseases and the Department of Microbiology & Immunology at the University of Michigan
  • Best practices to recover from an out-of-control event
    JUN 30, 2021 8:00 AM PDT
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    Best practices to recover from an out-of-control event
    Lorin Bachmann, Ph.D.
    Virginia Commonwealth University, Richmond, VA
  • APR 07, 2021 8:00 AM PDT
    Questions about Quality Control? Ask our Expert Panel
    David G. Grenache, PhD, MT(ASCP), D(ABCC), FAACC, Mark A. Cervinski, PhD, DABCC, FAACC, Joely Straseski, PhD, MS, MT(ASCP), DABCC, Nikola Baumann, PhD, DABCC
    David G. Grenache, PhD, MT(ASCP), D(ABCC), FAACC
    Chief Scientific Officer, TriCore Reference Laboratories
    Mark A. Cervinski, PhD, DABCC, FAACC
    Director, Clinical Chemistry and Point-of-Care at the Dartmouth-Hitchcock Medical Center
    Joely Straseski, PhD, MS, MT(ASCP), DABCC
    Associate Professor, University of Utah School of Medicine & Medical Director, ARUP Laboratories
    Nikola Baumann, PhD, DABCC
    Director, Central Processing at Mayo Clinic & Co-Director, Central Clinical Laboratory
  • FEB 24, 2021 8:00 AM PST
    Best Practices for Lot Changes in Quality Control or Reagents
    John Yundt-Pacheco, MSCS, Nico Vandepoele, BSc
    John Yundt-Pacheco, MSCS
    Scientific Fellow, Bio-Rad Laboratories
    Nico Vandepoele, BSc
    Scientific and Professional Affairs Manager, Bio-Rad Laboratories
  • Cost of Quality and the Medical Laboratory 2020
    NOV 18, 2020 11:00 AM PDT | NOV 19, 11:00AM SGT | NOV 19, 4:00PM CET
    Cost of Quality and the Medical Laboratory 2020
    Lucia M. Berte, MA, MT(ASCP)SBB, DLM; CQA(ASQ)CMQ/OE
    Principal, Laboratories Made Better!
  • The benefit of using an independent Quality Control
    OCT 21, 2020 11:00 AM PDT | OCT 22, 11:00 AM SGT | OCT 22, 4:00 PM CEST
    The benefit of using an independent Quality Control
    Abobaker Mohamed Yagoot, MT (ASCP), MLT (CMLTO)
    Supervisor Biochemistry (King Abdulaziz Medical City, National Guard Hospital - Jeddah- Saudi Arabia)
  • How to Limit Patient Harm from Erroneous Results, QC Strategies Based on Risk Management
    SEP 16, 2020 11:00 AM | SEPT 17, 11:00 AM SGT | SEPT 17, 4:00 PM CEST
    How to Limit Patient Harm from Erroneous Results, QC Strategies Based on Risk Management
    John Yundt-Pacheco, MSCS
    Scientific Fellow, Bio-Rad Laboratories
  • AUG 26, 2020 11:00 AM PDT | AUGUST 27, 11:00 AM SGT | AUGUST 27, 4:00 PM CEST
    SARS-CoV-2 Quality Control for Molecular and Serology assays
    Duane Newton, PhD, D(ABMM), FIDSA, Elitza S. Theel, PhD, D(ABMM)
    Sponsored By: Bio-Rad Laboratories
    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
  • Best Practices in Quality Control: 10 Simple Recommendations
    JUL 15, 2020 11:00 AM PDT
    Best Practices in Quality Control: 10 Simple Recommendations
    Curtis Parvin, PhD
    Biostatistical Advisor
July 2020 - July 2021
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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

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Speakers

  • Lorin Bachmann, Ph.D.
    Virginia Commonwealth University, Richmond, VA
    Biography

      Dr. Bachmann is Associate Professor of Pathology and Co-Director of Clinical Chemistry at Virginia Commonwealth University Medical Center. She is currently serving on numerous committees including the American Association for Clinical Chemistry (AACC) Finance and Nominating Committees and the College of American Pathology (CAP) Accuracy Based Programs Committee. Dr. Bachmann also serves as a member of the NIDDK/IFCC Laboratory Working Group for Standardization of Albumin in Urine, and is Chair of the Clinical and Laboratory Standards Institute (CLSI) Expert Panel on Clinical Chemistry and Toxicology. Dr. Bachmann's research and clinical interests include development of laboratory practice guidelines, standardization of clinical laboratory assays and quality assurance. She has provided numerous workshops, continuing education sessions and seminars on quality assurance and other laboratory-related topics.

    • Nikola Baumann, PhD, DABCC
      Director, Central Processing at Mayo Clinic & Co-Director, Central Clinical Laboratory
      Biography

        Dr. Baumann is Co-Director of the Central Clinical Laboratory and Director of Central Processing at the Mayo Clinic in Rochester, MN. Dr. Baumann received her PhD in Biochemistry from the University of Wisconsin-Madison. She then completed a Clinical Chemistry Fellowship at Washington University School of Medicine in St. Louis and obtained board certification in clinical chemistry (ABCC). Her specific area of interest includes improving quality in the automated clinical laboratory. Dr. Baumann was the faculty chair for the AACC Certificate Program on Patient Safety Essentials for Laboratory Professionals.  She served on the CLSI Document Development Committee on Statistical Quality Control (C24) and was a faculty contributor to the AACC Certificate program on Quality Control in the Clinical Laboratory. Dr. Baumann is committed to education and teaching.  She currently is the program director of the Mayo Clinic Clinical Chemistry Fellowship Program.

      • Mark A. Cervinski, PhD, DABCC, FAACC
        Director, Clinical Chemistry and Point-of-Care at the Dartmouth-Hitchcock Medical Center
        Biography

          Dr. Cervinski is the Director of Clinical Chemistry and Point-of-Care at the Dartmouth-Hitchcock Medical Center in Lebanon, New Hampshire, and Associate Professor of Pathology and Laboratory Medicine at the Geisel School of Medicine at Dartmouth, in Hanover, New Hampshire. During Dr. Cervinski's time at DHMC, the laboratory volume in chemistry has more than quadrupled as the hospital has affiliated with numerous critical access hospitals and outpatient clinics. He developed a clinical chemistry fellowship program that attained ComACC accreditation in 2015, and has trained four fellows to date, with two more in training. He is actively involved in the education of pathology residents and has served on the departmental Clinical Competency Committee for the past four years, and recently completed his first year as the Chair of the committee. Additionally, Dr. Cervinski developed DHMC's moving averages program that detects shifts in assay performance long before the next scheduled quality control event.

        • David G. Grenache, PhD, MT(ASCP), D(ABCC), FAACC
          Chief Scientific Officer, TriCore Reference Laboratories
          Biography

            Dr. Grenache is the chief scientific officer for TriCore Reference Laboratories in Albuquerque, New Mexico. In that role, he leads the TriCore Research Institute and works cooperatively to develop and implement TriCore's scientific research strategy. He is also the medical director of the chemistry, immunology, and esoteric analytic chemistry labs, a clinical professor of pathology at the University of New Mexico, and president of the American Association for Clinical Chemistry. He is a diplomate of the American Board of Clinical Chemistry and a Fellow in the AACC Academy. His research interests are centered on leveraging longitudinal laboratory data to gain insights into population health and the diagnostic tests used to manage the pregnant patient.

          • Adam Lauring, MD, PhD
            Associate Professor in the Department of Internal Medicine/Division of Infectious Diseases and the Department of Microbiology & Immunology at the University of Michigan
            Biography

              Dr. Adam Lauring is an Associate Professor in the Department of Internal Medicine/Division of Infectious Diseases and the Department of Microbiology & Immunology at the University of Michigan. He received his undergraduate degree from the Yale University and his MD and PhD from the University of Washington in Seattle. Dr. Lauring pursued his post-graduate clinical and research training at the University of California, San Francisco, where he completed a medical residency, an Infectious Diseases fellowship, and a postdoctoral fellowship in virology. He also served as Chief Medical Resident in the Department of Medicine. He has been on the faculty at the University of Michigan since 2012. Dr. Lauring studies the fundamentals of how viruses mutate and how this drives the evolution of poliovirus and influenza virus. His more recent work utilizes advanced sequencing of patient samples to define how viruses transmit in households and escape host immunity. He is using a similar approach to understand how SARS-CoV-2 evolves within hosts and spreads between them. Dr. Lauring is a Fellow of the Infectious Diseases Society of America and a member of the governing council of the American Society for Virology. His research on respiratory viruses has been funded by grants from the NIH, CDC, the Burroughs Wellcome Fund, and the Bill and Melinda Gates Foundation.

            • Joely Straseski, PhD, MS, MT(ASCP), DABCC
              Associate Professor, University of Utah School of Medicine & Medical Director, ARUP Laboratories
              Biography

                Dr. Straseski is an Associate Professor of Pathology at the University of Utah School of Medicine. She is the section chief of clinical chemistry and medical director of endocrinology and automated core laboratories at ARUP Laboratories, a national reference laboratory in Salt Lake City, Utah.  She is board certified in clinical chemistry by the American Board of Clinical Chemistry and is a fellow of the AACC Academy. Dr. Straseski received her Ph.D. in pathology and laboratory medicine from the University of Wisconsin-Madison and completed a postdoctoral fellowship in clinical chemistry at the Johns Hopkins Medical Institutions in Baltimore, Maryland.  She is an active member of and holds leadership positions within the American Association for Clinical Chemistry and the American Society for Clinical Pathology.

              • Lucia M. Berte, MA, MT(ASCP)SBB, DLM; CQA(ASQ)CMQ/OE
                Principal, Laboratories Made Better!
                Biography

                  Ms. Berte has always been interested in laboratory quality management, having served as a blood bank manager and the laboratory's quality coordinator. She teaches medical laboratories around the world how to implement a Quality Management System (QMS), use it to improve patient safety, and use it to reduce the cost of poor quality. She also trains laboratorians how to write better documents and how to design more effective training and competence assessment programs. Ms. Berte has a Bachelor of Science degree in Medical Technology and a Master of Arts Degree in Health Care Administration. In addition to being an American Society for Clinical Pathology certified medical technologist, specialist in blood banking and diplomate in laboratory management, she is also certified as a quality manager and quality auditor by the American Society for Quality. Ms. Berte has volunteered for the Clinical and Laboratory Standards Institute (CLSI) for over 25 years in roles such as chairholder of the QMS Subcommittee, chairholder of many CLSI QMS guidance documents, and member of several past and current document development committees. She was the co-leader for ISO TC-212 Work Group 1 for the ISO 15189:2012 international medical laboratory standard and serves on the standard's drafting team for the upcoming ISO 15189 revision. She has been the author of numerous articles, chapters, and books and continues to provide audioconferences, workshops, and learning courses on various aspects of laboratory quality.

                • 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. 

                      • Nico Vandepoele, BSc
                        Scientific and Professional Affairs Manager, Bio-Rad Laboratories
                        Biography

                          Mr. Nico Vandepoele serves as Scientific and Professional Affairs manager for the Bio-Rad Laboratories Quality Control Division. He works to promote an understanding of laboratory regulations and best practices as they pertain to QC and EQA/PT programs. Nico is a well-recognized speaker and presents trainings, workshops and lectures at symposia around the world and volunteers on several CLSI committees.

                          Nico studied in Bruges Belgium in the Higher Technical Institute and graduated in 1995 as a Bachelor in Clinical Chemistry with a dual degree in Information Technologies and Chemistry. He worked in a clinical lab for and then for a Biotech company as head of the research lab before starting at Bio-Rad as Field Application Specialist. In 2010, Nico became product manager for the Quality Systems Division in Irvine, California where he managed the Unity and EQAS informatics programs.

                        • Abobaker Mohamed Yagoot, MT (ASCP), MLT (CMLTO)
                          Supervisor Biochemistry (King Abdulaziz Medical City, National Guard Hospital - Jeddah- Saudi Arabia)
                          Biography

                            Mr. Abobaker Yagoot has a background in Biochemistry. He obtained his Bachelor of Science in Biochemistry from Ain Shams University, Cairo in Egypt. He received the Medical Laboratory Technology Certificate from St. Clair College-Windsor from Ontario, Canada in 1992. He also obtained the certification for Medical Technologist (M.T – A.S.C.P) from American Society of Clinical Pathologist, New York State, USA. Prior to his current position at the National Guard Health Affairs, he had a key role in the Quality Assurance/Quality Improvement Office at the Chemistry Department of King Faisal Specialist Hospital and Research Centre. Mr. Abobaker Yagoot is actively involved in conferences nationally and internationally. In addition to those roles, Mr Abobaker Yagoot is a Certified C.A.P. inspector.

                          • 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


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