The Regulation of Veterinary Medicine

• Which way now in Europe: National marketing approval, mutual recognition or the centralised procedure?

• European data requirements: What goes where in each section of the submission?

• US FDA procedures: How to file in the US

• US FDA data requirements: The local specifics

• Regulations in Japan: Understand the potential of your global market

For Animal Health Specialists:

This course will explain the detailed regulatory requirements in the US, Europe and Japan. It will ensure you have up-to-date, accurate knowledge of the markets in which you work - whether now or in the future. You will gain a thorough understanding of regulatory procedures specific to the veterinary sector and have a clear view of the global market. Ask the right questions, know the right answers and get your drug to market.

For Regulatory Affairs Professionals:

The veterinary medicines market is an important one. The products authorised for use in animal health are as complex as those for human pharmaceuticals and often even more heavily scrutinsed. The Regulation of Veterinary Medicines will give experienced hands an update, with all the major global regulations in one place, while new recruits will benefit from instant and in-depth knowledge of these major global markets.