Training courses & Webinars:
Animal Health

Management Forum 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.

 

Please note: full product details will be shown on our training portal IPI Academy where you can find out more and book

A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products Training Course

A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products

7 May 2026 - Online webinar
Also on: 3 Nov 2026

Understanding the chemistry, manufacturing and controls (CMC) requirements for veterinary pharmaceuticals is essential to support successful registration in the EU.

Presented by Craig Evans (bio)
Dave Parry (bio)

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A Practical Approach to Veterinary Vaccine Development and Registration in the EU (European Union) Training Course

A Practical Approach to Veterinary Vaccine Development and Registration in the EU

6-7 Nov 2025 - Online webinar
Also on: 10 Mar 2026

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 Michael Fontaine (bio)
Mel Munro (bio)

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Advanced Veterinary Pharmacovigilance Training Course

Advanced Veterinary Pharmacovigilance

21-22 May 2026 - Online webinar
Also on: 4 Nov 2026

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.

Presented by Declan O'Rourke (bio)

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Animal Feed and Feed Additive Registration in China and Thailand Training Course

Animal Feed and Feed Additive Registration in China and Thailand

16 Apr 2026 - Online webinar
Also on: 22 Oct 2026

Learn how to navigate the regulatory system for animal feed and feed additives in two emerging markets.

Presented by Bi Jun (bio)
Anongrut (Mai) Surarutrungsri (bio)

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Introduction to Veterinary Pharmacovigilance Training Course

Introduction to Veterinary Pharmacovigilance

9-10 Mar 2026 - Online webinar
Also on: 16 Sep 2026

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.

Presented by Declan O'Rourke (bio)

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Managing Service Providers including CRO (Contract Research Organisation) and CMOs oversight to comply with ICH GCP (Good Clinical Practice) R3 Training Course

Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3

13-14 Apr 2026 - Online webinar
Also on: 15 Oct 2026

Optimising oversight for inspection compliance.

Presented by Laura Brown (bio)

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Practical Implementation of GCP (Good Clinical Practice) in Veterinary Field Studies Training Course

Practical Implementation of GCP in Veterinary Field Studies

25-26 Nov 2025 - Online webinar
Also on: 13 May 2026

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 (bio)
Jenny Webster (bio)

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Registration of Veterinary Pharmaceuticals in China Training Course

Registration of Veterinary Pharmaceuticals in China

16 Apr 2026 - Online webinar
Also on: 22 Oct 2026

Learn how to navigate the regulatory system of veterinary pharmaceuticals in China.

Presented by Bi Jun (bio)

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The Animal Health Summer School: Working Through Veterinary Drug Development in the EU (European Union) and USA Training Course

The Animal Health Summer School: Working Through Veterinary Drug Development in the EU and USA

15-18 Jun 2026 - London

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

Presented by Andrew Hewitt (bio)
David Petrick (bio)

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Veterinary Pharmaceutical Submissions in the EU (European Union) Training Course

Veterinary Pharmaceutical Submissions in the EU

25-26 Nov 2025 - Online webinar
Also on: 18 May 2026

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 (bio)
Dave Parry (bio)

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Content was good, speaker was knowledgeable and the pace was good.

Richard Pringle, Associate Director of Regulatory Affairs, Univet Ltd

The speaker was clear and concise and very willing to answer any questions with patience.

Richard Pringle, Associate Director of Regulatory Affairs, Univet Ltd

The Speaker was very well informed, clear in his presentation technique and keen and quick to address any questions. The content, pace and flow of the webinar was well judged and the way we were provided with examples of signals was very useful.

Richard Pringle, Associate Director of Regulatory Affairs, Univet Ltd

A 10 overall. I hoped to have an overview of pharmacovigilance, learning the most relevant points. It has pleasantly fulfilled my expectations.. Despite not being 100% fluent in English, I could understand [speaker] quite well as he explained himself in a way that captured something as big as pharmacovigilance-very well.

Miranda Sandoval Díez , QPPV, Laboratorios Syva Sa

This was a comprehensive webinar training that met my expectations: highly illustrated with examples, interactive, enabling experience sharing with other attendees. All parts were complete and great speaker. I really appreciated the introduction of tools and templates that are helpful.

katia Hay, Clinical trial coordinator, Adocia

My goal was to gain a deeper awareness and understanding of what is required in the different sections of a dossier for submission in the EU. I think the course definitely accomplished this and there was lots of useful information, which was very well explained. I can confidently say that I left knowing a lot more than I initially thought I would.

Emilija Stabingyte, Regulatory & Quality Coordinator, Zoetis UK Limited

Fantastic webinar! Speakers were very knowledgeable, clear, concise, and open to questions at any time—providing in depth background information were appropriate as well. The content was very interesting and I think a very good amount was covered considering the timescales. I enjoyed the workshop a lot. I thought it was a good way to try and put into practice what we had learnt during the webinars. I also thought a very good amount of information was covered for an introduction into the sections of the dossier.

Emilija Stabingyte, Regulatory & Quality Coordinator, Zoetis UK Limited

It was well laid out and formatted especially for myself who does not have a regulatory role currently. I was hoping to achieve a firmer understanding and overview of submission within the EU, and believe I achieved this. [Speakers] were very knowledgable and provided great answers to all questions— supportive but challenged us when doing the workshop. I liked all areas of the course.

Louise Dunn, Pharmacovigilance and Technical advisor, Zoetis

Overall, the course is very good. The speaker is very kind and answers the participants’ questions patiently and clearly. It’s evident that he masters the subject and has faced the same challenges and doubts that we, as participants, encounter in our daily work. It was also great that he helped us with practical examples and gave us tips to reduce the workload in some areas.

Elisabet Roca, Marketing and Business Strategy, FEEKA ANIMAL HEALTH

It was clear that Laura is very experienced within the field. Good presentations, and she tried to make it interactive.

Debbie Grønlund, QA Compliance Specialist, Sanos Group