Pharmacovigilance in Animal Health
March 24
8:30 a.m. to 4 p.m. CT
Options for online and in-person
Workshop Description
The Pharmacovigilance in Animal Health workshop provides attendees with an understanding of what pharmacovigilance is and what it means to the Center for Veterinary Medicine/U.S. Food and Drug Administration and the Center for Veterinary Biologics/U.S. Department of Agriculture. Both agency's reporting process will be covered and what to be aware of with recent changes.
Attendees also will gain an understanding of the global perspective as it relates to both VICH and non-VICH regulated products and have an opportunity to apply what they've learned to real-life case studies.
Dr. Jane Owens received a B.S. in Animal Science from the University of Kentucky and her D.V.M. from Tuskegee University, School of Veterinary Medicine. She completed her doctoral training in equine pharmacology at the department of veterinary physiology, pharmacology and toxicology at Louisiana State University and her doctoral fellowship at the Chemical Industry Institute of Toxicology, Research Triangle Park, North Carolina. 
Dr. Kara Raetzel is currently a senior technical consultant at Elanco Animal Health, where she provides technical support to both veterinarians and pet owners as well as the reporting and investigation of potential product related adverse events. Prior to working at Elanco, she held a similar position at Bayer Animal Health, where she also provided technical and medical review of marketing pieces. She entered industrial veterinary medicine following 15 years of companion animal practice after obtaining a veterinary degree at Kansas State University.
Dr. John Schiltz received his D.V.M. degree from Iowa State University. Work experience includes private practice, State Veterinarian for Iowa, Diagnostic Virology Lab, Swine Program staff and currently with the Center for Veterinary Biologics. Dr. Schiltz will discuss the requirements and implications of the new mandatory adverse event reporting regulation.
With a veterinary degree from the University of Montreal, Dr. Martin Tiemann spent 20 years in mixed animal practice between Montreal and Ottawa in Canada. He joined Industry with Merial Canada as the manager of RA, QA and Technical Services. Martin came to the U.S. to take a director of pharmacovigilance and product stewardship with Intervet in Delaware. Following a series of acquisitions by Schering Plough and then Merck, Martin chose to move to the Midwest in 2009 to work for Boehringer Ingelheim, he has had several roles in RA and PV, including serving as the head of global pharmacovigilance from 2018 to 2020. Since November 2020, Martin is the head of Pharmacovigilance and Veterinary Technical Services NA at Boehringer Ingelheim Animal Health U.S.
Registration
Individual cost
- $800 per person
Group rate
Group discounts are available for three or more employees per company. Contact Lauren Racki at laurenracki@ksu.edu or 913-307-7340 to obtain discount codes for a group.
Series registration
Register for the 2022 Regulatory Affairs in Animal Health Seminar Series and receive a discount of 10%, or $800 (this equates to a free one-day workshop).
The 2022 series consists of the Pharmacovigilance in Animal Health; Animal Health Regulatory 101; Advanced Animal Biologics; Deviations, Root Cause Investigations and CAPA in Animal Health; Pesticides in Animal Health; and Advanced Animal Pharmaceutical workshops, as well as the Dissolution and Roadmap to Market: Supply Chain in Animal Health seminars.