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Three Day Online Seminar: Veterinary Drug Approval Process and FDA Regulatory Oversight (June 9-11, 2021) – ResearchAndMarkets.com

DUBLIN–(BUSINESS WIRE)–The “The Veterinary Drug Approval Process and FDA Regulatory Oversight” conference has been added to ResearchAndMarkets.com’s offering.

The U.S. Food and Drug Administration’s Center for Veterinary Medicine (CVM) is responsible for the approval of veterinary drug products intended for family pets, food-producing animals, and other animal species.

This seminar will cover the process for obtaining federal government approval for marketing new animal drug products that are under the jurisdiction of the FDA, and also briefly covers animal products that are regulated by other federal agencies. For example, animal vaccines, animal disease diagnostic devices and some animal biologics are regulated by the U.S. Department of Agriculture, and some flea and tick control products are regulated by the Environmental Protection Agency.

This two-day interactive seminar will provide attendees with an understanding of the FDA’s veterinary drug approval process. The group size is small, generally between 8 and 20 people, with plenty of opportunities to ask questions and discuss issues or challenges that the attendees have experienced.

Learning Objectives:

Key goals of the seminar will include learning:

Who Should Attend:

This course is designed primarily for people tasked with developing new animal drugs for an animal health company or a human pharmaceutical company. This includes individuals responsible for overseeing regulatory affairs, developing veterinary drug products, or evaluating new technologies or applications. Among others, this includes:

Agenda:

Day 01 (9:00 AM to 1:00 PM PDT)

Day 02 (9:00 AM to 1:00 PM PDT)

Day 03 (9:00 AM to 1:00 PM PDT)

For more information about this conference visit https://www.researchandmarkets.com/r/m9emns

Contacts

ResearchAndMarkets.com

Laura Wood, Senior Press Manager

press@researchandmarkets.com
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