AAVPT Veterinary Drug Regulatory Life Cycle (A to Z) Day 3 of 5
Basic information on AAVPT Workshop
The FDA Center for Veterinary Medicine (CVM) recognizes that drug sponsors, regulatory scientists in industry and academia, new CVM employees, and other CVM stakeholders need a better understanding of regulatory science, particularly CVM’s new animal drug approval process. To address this need, CVM has created an all-inclusive course on the new animal drug approval process and post-approval evaluation entitled “AAVPT Veterinary Drug Regulatory Life Cycle (A to Z).”
The week-long course is a comprehensive overview of CVM regulatory processes for new animal drug approvals and post-approval surveillance and compliance of marketed drugs. The course will cover topics related to current policies, procedures, and standards across all technical sections of the drug approval process and all other aspects of the veterinary drug life-cycle. Attendees will be introduced to all of CVM’s groups and activities and will have opportunity to interact with scientists from various CVM offices and divisions.
The course content is targeted to stakeholders in industry and academia who are interested in understanding the regulatory science of veterinary drug development. Scientists,in all areas of drug research and development, manufacturing, and clinical testing, may benefit from taking this course.