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

5 Nov 2024 - Online webinar

Understanding the chemistry, manufacturing and controls (CMC) requirements for veterinary pharmaceuticals is essential to support successful registration in the EU. Regulations for CMC of veterinary pharmaceuticals are complex and are regularly updated, making pharmaceutical product development challenging. This course is designed to guide you through the essential steps in development of the formulation and manufacturing process, in a manner that will ensure regulatory compliance for clinical trial applications and marketing authorisation applications.

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

8-9 Jul 2024 - Online webinar
Also on: 11 Nov 2024

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 Mel Munro (bio)

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Advanced Veterinary Pharmacovigilance Training Course

Advanced Veterinary Pharmacovigilance

30 Apr-1 May 2024 - Online webinar
Also on: 2 Jul 2024

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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Introduction to Veterinary Pharmacovigilance Training Course

Introduction to Veterinary Pharmacovigilance

26-27 Jun 2024 - Online webinar
Also on: 2 Oct 2024

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.

*INCLUDES: Interactive workshop and discussion sessions*

Presented by Declan O'Rourke (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

19-20 Mar 2024 - Online webinar
Also on: 15 Jul 2024

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.

Presented by Rachel Anderson (bio)
Donna Taylor (bio)
Jenny Webster (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

17-20 Jun 2024 - 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

11-12 Jul 2024 - Online webinar
Also on: 26 Nov 2024

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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Very nice. I would recommend.

Magali Rigo, RA Pharma Manager, Boehringer Ingelheim Animal Health

I thought it was overall a very good course that I would recommend people to take.

Marte Sønnervik, Clinical Study Coordinator, PHARMAQ

I'm very delighted with the course, the presentation and the speakers.

Cuong Nguyen, Associate Specialist, Clinical Research, MSD Animal Health Innovation GmbH

Excellent and engaging content using some 'real life' examples which offered context for greater insight, delivered by an experienced presenter who was able to provide additional depth when further questions were asked.
I thoroughly enjoyed it thank you!

Claire Francis, LRRP and Regulatory Affairs Officer, Vetoquinol UK Ltd

Every item, but especially the topics of signal management & audits and inspections. I am grateful for the advise giving on how to approach audits/inspections.

Charlotte Lindorf Eriksen, Head of Pharmacovigilance, QPPV, Billev Pharma ApS

The presentations were clear and precise and a good source for information after the the training.

Gabriele Hoesch, Manager Quality Transfer, Launch & Projects, Boehringer Ingelheim Vetmedica GmbH

I am very happy to have been on this course. It was very beneficial to my work.

Ciara Cousins, Clinical Vet and Veterinary Advisor, Norbrook

I wanted to get some good practices on how to manage dossier from a strategic and admin standpoint. Recommendations were given during the training so I think info I wanted to get was given.

Karine Tanan, Principal Scientist, Scientific and Regulatory Affairs, Cargill R and D Centre Europe

I really enjoyed the course and Rachel, Jenny and Donna were wonderfully engaging presenter and given us lots of opportunity to ask the questions. The course was mix of theory & few practical exercises. I took away lots of things which I can easily apply at my work .

Kritika Sengar Chauhan, Associate Specialist, Clinical Research, MSD Animal Health Innovation GmbH

It was a very good training regarding all aspects: organisation, speakers, documents, timing. A lot and very useful information.

Yasmina Mallouk , Quality Assurance Auditor , Boehringer Ingelheim