Best Practices for Lot Changes in Quality Control or Reagents

Presented By: John Yundt-Pacheco, MSCS, Nico Vandepoele, BSc
Speaker Biography:
John Yundt-Pacheco: 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.
Nico Vandepoele, BSc: 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.
Webinar: Best Practices for Lot Changes in Quality Control or Reagents
Webinar Abstract: Starting a new quality control or reagent lot is a critical point in the workflow of a lab. Standard clinical laboratory practices can vary during this process and these changes have the potential to adversely affect patient results and lab operations. To ensure your laboratory produces consistent patient results, this webinar will present the most recent developments and best practices to perform quality control and reagent cross-over studies.
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