Training format
Topic
Live online, Classroom
Presentations will cover the regulatory framework, pharmaceutical, toxicological and pharmacological data, safety risk assessments, pre-clinical and clinical data, critical expert reports and regulatory submissions.
Presented by Andrew Hewitt
and Dave Parry
Live online
This event has been designed to give practical advice and guidance on how to successfully develop market approval in the EU. The programme will take participants through a step-by-step approach to the process and will also provide key guidance on how to maintain MA once achieved.
Presented by Dr Mel Munro
Summer school
Classroom
This practical four-day course provides a comprehensive understanding of veterinary medicine development in the EU and USA.
Presented by Andrew Hewitt
and David Petrick
Live online, Classroom
This 2-day training course offers practical advice and real-world troubleshooting for those involved in the design, conduct, monitoring, recording, auditing, and reporting of VICH GCP compliant clinical studies.
Presented by Donna Taylor
and Jenny Webster
Live online
Understanding the chemistry, manufacturing and controls (CMC) requirements for veterinary pharmaceuticals is essential to support successful registration in the EU.
Presented by Mr Craig Evans
and Dave Parry
New for 2026
Live online
Learn how to navigate the regulatory system of veterinary pharmaceuticals in China.
Presented by Bi Jun
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