Animal Drug Approval Process

Seminar Speaker

Overview of Clinical and Regulatory Development for FDA Veterinary Drug Approval

Mark Hughes, DVM, MS

Mark Hughes has over 13 years of experience in veterinary drug product development and extensive experience in university veterinary research, laboratory animal medicine, and development of in-vitro diagnostic tests. Dr. Hughes has managed or contributed to clinical studies and regulatory submissions on the safety and effectiveness of veterinary drugs (including stem cell therapies) for therapeutic treatments related to dermatology, cardiology, endocrinology, oncology, osteoarthritis, and infectious diseases. Through his consulting business, Hughes Veterinary Consulting, he has been assisting domestic and international biotech and pharmaceutical companies with the process of obtaining FDA regulatory approval of drug products for use in companion animals.

Dr. Hughes has presented similar educational seminars for ComplianceOnline, both in-person in major cities such as Kansas City and Houston, and virtually in webinars since the COVID epidemic started. For these new in-person seminars managed by HVC, our goal is to conduct the meetings at unique locations with enhanced appeal and things to do and places to see before and after the meetings. Group size is limited to 18 people to allow plenty of interaction and discussion between participants.

A summary of Dr. Hughes' work experience is posted on LinkedIn: http://www.linkedin.com/in/markhughesdvm

Hughes Veterinary Consulting (HVC)

760-315-1130 (Text or Voice)