Charles River’s site in Mattawan, Michigan, performs general toxicology studies and specialized studies such as DART, ototoxicity, ocular toxicology, and abuse liability. The facility also supports the development of medical devices and gene and cell therapies.
Meet the Team
The addition of experts and scientists from MPI Research brings fresh perspectives and years of experience to our growing Safety Assessment team. Take a moment for a quick “meet and greet” with a few of our new team members.
Theodore Baird, PhD, DSP, Sr. Director of Safety Evaluation & Principal Study Director
Theodore Baird, PhD, DSP, serves as Senior Director of Safety Evaluation, and as a Principal Study Director at Charles River. He is also an adjunct professor in the Biomedical Sciences Department at Western Michigan University. Dr. Baird received his PhD in biological psychology from the University of Oklahoma Health Sciences Center in 1998, and came to MPI Research following a postdoctoral research fellowship in the Department of Pharmacology at the University of Michigan. As an expert with 18 years of pharmaceutical industry experience, Dr. Baird has authored more than 450 reports on proprietary compounds with respect to cardiovascular, renal, gastrointestinal, central nervous and respiratory system safety and/or efficacy, as well as conducting a wide range of regulatory general toxicology studies in mice, rats, rabbits, guinea pigs, dogs, swine, and nonhuman primates. Dr. Baird’s publication record includes over 165 presentations, abstracts, and/or manuscripts. He is presently a member of the American College of Toxicology, as well as a current member and Diplomate of the Safety Pharmacology Society.
Dan Patrick DVM, DACVP, DABT, Toxicologic Pathologist & Director of Pathology
Dan Patrick DVM, DACVP, DABT is a toxicologic pathologist and the Director of Pathology at Charles River. He received his DVM from Iowa State University, completed anatomic pathology residency training at Michigan State University, and is board certified by the American College of Veterinary Pathologists (ACVP) and the American Board of Toxicology (ABT). He has broad experience with the safety assessment of a wide variety of laboratory animal species and study types and promotes integration between pathologists, cross functional areas, external scientists, and Sponsors; providing problem-solving and mediation as needed. He has authored many scientific articles and textbook chapters and enjoys educational outreach, serving as an adjunct professor in the College of Veterinary Medicine at Michigan State University and serving as coordinator for the toxicologic pathology residency program at Michigan State University. Currently he is serving as an ACT Councilor and member the Society of Toxicologic Pathology’s (STP) Scientific and Regulatory Policy Committee which provides focus and perspective on scientific and regulatory issues which are pivotal to the practice of toxicologic pathology. Other ACT activities include serving as a liaison between the ACT and STP, organizer for ACT “Pathology for Non-Pathologists” courses, and has presented at ACT Annual Meetings and webinars. He is a member of the STP, ACT, SOT, ACVP, European Society of Toxicologic Pathology, and the American Veterinary Medical Association.
Thomas Vihtelic, DVM, PhD, Director & Sr. Study Director of Experimental Therapeutics
Thomas Vihtelic, DVM, PhD joined MPI Research in 2008 as a Study Director in Targeted Discovery Research and now serves as Director and Senior Study Director of Experimental Therapeutics. Dr. Vihtelic assists Sponsors in the design of preclinical studies in support of ophthalmology, inflammation, parasitology, and infectious disease therapies. Before joining MPI Research, he was a Research Associate Professor of Biology at the University of Notre Dame using molecular genetic strategies to study eye lens development and establishing a model of light-induced photoreceptor degeneration to characterize adult stem cell roles in the regenerating zebrafish retina. Dr. Vihtelic received a DVM from Michigan State University and a doctorate in molecular genetics from the University of Notre Dame. His doctoral research, which focused on characterization of Drosophila retinal degeneration genes, was followed by postdoctoral work at the University of Chicago (Department of Ophthalmology and Visual Sciences) and the Massachusetts Eye and Ear Infirmary (Howe Laboratory of Retina Molecular Genetics and Harvard Medical School) using mouse retinal degeneration mutants and transgenic lines. Dr. Vihtelic has presented and published in the field of experimental ophthalmology and maintains memberships in the Association for Research in Vision and Ophthalmology and American Association of Veterinary Parasitologists.
Rachel Tapp, MS, LATG, Sr. Study Director of Neurobehavioral Sciences
Rachel Tapp, MS, LATG, is a Senior Study Director in neurobehavioral sciences at Charles River. As an expert with more than 15 years of experience, she ensures high level performance of regulatory and non-regulatory contracted neurobehavioral ototoxicity studies, focusing on study management, communication, and fostering Sponsor relationships. Ms. Tapp joined MPI Research in 2003 as a research associate and was promoted to Study Director in 2005. Before joining the company, she worked as a field research technician at the National Audubon Society and as a laboratory assistant in the Aquatic Toxicology Laboratory at Michigan State University. Ms. Tapp obtained her BS in zoology from Michigan State University in Michigan in 2002, and her MS in Pharmacology and Toxicology from Michigan State University in 2016. She has authored many auditory safety posters and articles and is an active member of the Association for Research in Otolaryngology, the Society for Neuroscience, and the Safety Pharmacology Society.