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2020 - The Veterinary Drug Approval Process and FDA Regulatory Oversight

Date2020-05-14 - 2020-05-15


VenueKansas City, MO, USA - United States USA - United States

KeywordsCenter for veterinary medicine; New animal drug application; Veterinary drug user fees


Topics/Call fo Papers

How the U.S. Food and Drug Administration (FDA) regulates animal drug products.
How FDA’s Center for Veterinary Medicine is organized.
The process by which veterinary drug products are reviewed and approved.
How to open an Investigational New Animal Drug (INAD) File.
The FDA’s various user fees, what fee waivers are available, and how to request a fee waiver.
The various technical sections included in a New Animal Drug Application (NADA).
What information is needed to substantiate product characterization, target animal safety and effectiveness.
An overview of FDA’s rules governing chemistry, manufacturing and controls (CMC).
The various components of an animal field study to support product approval.
How animal feed, veterinary devices, OTC drug products and nutritional supplements are regulated in the U.S.

Last modified: 2020-04-30 02:54:59