Hosted by: The Regulatory and Safety Evaluation (RSESS) and Comparative Toxicology, Pathology, and Veterinary Toxicology (CTPVSS) Specialty Sections
Registration is required for this free webinar
This webinar will provide an overview of non-clinical safety data requirements for veterinary drugs, including ‘Novel Therapies’, in the UK, incorporating VICH requirements. Participants will gain insights into the distinct regulatory considerations for both companion animals and food-producing species, exploring the nuanced safety evaluation approaches required for each category. Additionally, the webinar will highlight some of the emerging opportunities to incorporate New Approach Methodologies (NAMs) and apply the 3Rs principles (Replacement, Reduction, Refinement) in veterinary drug development. This informative presentation is designed for toxicologists, regulatory professionals, researchers, and others involved in veterinary pharmaceutical development seeking to navigate the complex global regulatory landscape effectively.
Speaker:
· Samuel Fletcher, Head of the Human and Environmental Safety Team at Veterinary Medicines Directorate (VMD), UK
Registration is required for this free webinar