Kelly Coleman, Ph.D., DABT, ERT, RACDistinguished Toxicologist, Technical Fellow, Bakken Fellow at Medtronic
Kelly P. Coleman is a Distinguished Toxicologist at Medtronic where he provides preclinical product development support. He is a U.S. Expert on the ISO 10993 working groups responsible for medical device biocompatibility standards on skin irritation, sensitization, and toxicological risk assessment. In addition, he recently completed a 4-year term on the U.S. National Toxicology Program’s Scientific Advisory Committee on Alternative Toxicological Methods and is the Past President of the Society of Toxicology’s In Vitro and Alternative Methods Specialty Section. Kelly holds a Ph.D. in Toxicology from the University of Minnesota, is a Diplomate of the American Board of Toxicology, a European Registered Toxicologist, and is certified in regulatory affairs.
Case Study: Adhering to ISO 10993-23 for Irritation Testing, 9:50amView Session
Panel: Assessing The Future of In Vitro Testing, 11:35amView Session