2021 - The Veterinary Drug Approval Process and FDA Regulatory Oversight
Date2021-06-09 - 2021-06-11
Deadline2021-05-30
VenueVirtual Seminar, USA - United States
KeywordsCenter for veterinary medicine; New animal drug application; Veterinary medicine regulation
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.
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.
Other CFPs
- ACH Exception Processes Workshop
- 21 CFR Part 11 Compliance for SaaS/Cloud Applications
- Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR
- Latin America - Understanding Regulatory Compliance Requirements Across the Life Science Industry (Focus: Brazil, Mexico, Argentina)
- The Do's and Don'ts of Record Retention and Destruction
Last modified: 2021-05-17 03:40:43