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Annual two-day regulatory update on animal feed and feed additives in the EU, USA and China – now in its tenth successful year.

Learn how to prepare a Request for Proposal (RFP), evaluate and select the right CRO and establish procedures for vendor oversight for R&D projects you need to outsource

Managing Vendor/CRO/CMO Oversight

8-9 Oct 2020

Also on: 26 Apr 2021

This seminar will take many aspects of animal health and veterinary research and development through a typical clinical trial, and pay attention to compliance with Good Clinical Practice (GCP) as outlined in the two guidelines on safety and efficacy produced by FEDESA and the CVMP.

This course will take participants through all of the necessary steps to obtain marketing authorisation for a feed additive in the European Union.

The programme will offer a comprehensive introduction to the new EU Regulation (2019/6) and will address the changes and implications to the industry including marketing authorisations, submissions and dossiers.

INCLUDES: Interactive discussion sessions

This practical four-day course provides a comprehensive understanding of veterinary medicine development in the EU and USA.