Meet Our Panel of Experts
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Analytical impurity reference standards guide and govern the work in chemical sciences, ensuring consistency across a wide range of companies across pharmaceutical and medicinal R&D, forensic science and environmental analysis. As a result, when selecting the analytical standards for research and development of chemicals or calibration and ongoing quality control, there are a number of potential pitfalls that can risk the success of a project, reducing efficiency.
During this hour-long webinar, Joe Lackey, technical specialist at LGC and Toni Rantanen, quality manager at TRC, show how TRC chemistry planning groups’ robust approach to chemical synthesis and quality control has been designed to solve specific problems faced by customers when purchasing impurities used as analytical references. The webinar ends with a case study illustrating the consequences of using low-quality impurity standards.
Meet Our Panel of Experts
Dr Joe Lackey holds a PhD in oncology from the University of Dundee, Scotland and has worked as an LGC technical specialist for six years, during which time he has explored his significant interests in personalised medicine, cancer biology and toxicology.
Toni obtained his PhD at RWTH Aachen, Germany, and joined Toronto Research Chemicals Inc. in 2014 as a synthetic chemist. In 2015 he took on a role as a lab supervisor, and subsequently in 2019 he stepped into the shoes of quality manager.
