IPI Academy provides a wide range of animal health training courses that will give you access to leading experts and the latest information within this field. The regulations that apply to veterinary medicines are complex and our series of courses will help you comply with the regulations for a successful market strategy.
The animal health industry is a growing and constantly changing market as the result of new opportunities, legislation and regulation in veterinary medicines, vaccines, animal feed and feed additives. To be competitive in this field it is essential to keep up-to-date with the global regulatory requirements and have access to experts who interpret these requirements and provide practical advice on application. We provide training from an introductory to an advanced level in this area of life science.
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Including the main requirements of Volume IXB, an update on the proposed EU Regulation (2019/6) on Veterinary Medicinal Products and the impact of Brexit.
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Learn how to navigate the regulatory system for animal feed and feed additives in two emerging markets.
Summer school
Classroom
This practical four-day course provides a comprehensive understanding of veterinary medicine development in the EU and USA.
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A basic training course for those working on drug safety in the EU. This course has been designed to provide basic training and a good introduction to those concerned with veterinary pharmacovigilance.
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Understanding the chemistry, manufacturing and controls (CMC) requirements for veterinary pharmaceuticals is essential to support successful registration in the EU.
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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.
Live online, Classroom
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.
New for 2025
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Learn how to navigate the regulatory system of veterinary pharmaceuticals in China.
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Annual two-day regulatory update on animal feed and feed additives in the EU, USA and China.
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.
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