In-house & bespoke training:
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

In-house & bespoke training

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

Typically presented by Craig Evans (bio) , Dave Parry (bio)

Typical duration: 1 day
Pricing from £500 per attendee
Delivery: collaborative classroom

More @ IPI Academy

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

In-house & bespoke training

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.

Rated by attendees to the public programme

Typically presented by Mel Munro (bio)

Typical duration: 2 days
Pricing from £1,000 per attendee
Delivery: collaborative classroom

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Advanced Veterinary Pharmacovigilance

In-house & bespoke training

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.

Rated by attendees to the public programme

Typically presented by Declan O'Rourke (bio)

Typical duration: 2 days
Pricing from £1,000 per attendee
Delivery: collaborative classroom

More @ IPI Academy

Animal Feed and Feed Additive Registration in China and Thailand

In-house & bespoke training

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

Typically presented by Bi Jun (bio) , Anongrut (Mai) Surarutrungsri (bio) , Yang Zheng (bio)

Typical duration: Half-day days
Pricing from £350 per attendee
Delivery: collaborative classroom

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Interpersonal Project Management Skills for the Life Sciences Industries

In-house & bespoke training

This two-day interactive course covers the essential interpersonal skills needed to excel as a life sciences project manager.

Typically presented by Laura Brown (bio)

Typical duration: 2 days
Pricing from £800 per attendee
Delivery: collaborative classroom

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Introduction to Veterinary Pharmacovigilance

In-house & bespoke training

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.

Rated by attendees to the public programme

Typically presented by Declan O'Rourke (bio)

Typical duration: 2 days
Pricing from £1,000 per attendee
Delivery: collaborative classroom

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Practical Implementation of GCP in Veterinary Field Studies

In-house & bespoke training

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.

Rated by attendees to the public programme

Typically presented by Rachel Anderson (bio) , Donna Taylor (bio) , Jenny Webster (bio)

Typical duration: 2 days
Pricing from £1,000 per attendee
Delivery: collaborative classroom

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Registration of Veterinary Pharmaceuticals in China

In-house & bespoke training

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

Typically presented by Bi Jun (bio)

Typical duration: 90-minutes days
Pricing from £200 per attendee
Delivery: collaborative classroom

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Veterinary Pharmaceutical Submissions in the EU

In-house & bespoke training

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.

Rated by attendees to the public programme

Typically presented by Andrew Hewitt (bio) , Dave Parry (bio)

Typical duration: 2 days
Pricing from £1,000 per attendee
Delivery: collaborative classroom

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Training options

All of our course outlines are available:
Ready made for any number of participants or With a programme and presenters customised to your requirements
And in your preferred format, or combination:
Face-to-face training at your location or Webinar/interactive online

Previous attendees said...

“Excellent. I was hoping to refresh, add to and update my knowledge. The webinar was excellent to remind me of areas that I had been involved with many years ago and add knowledge that is more relevant to my role now. I found the topics of the workshop particularly relevant.”

Mary-Ann Tite, Regulatory Manager, Pets |Choice

“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

“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

“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

“I wanted to have a synthetic overview of part 3 and 4 and wanted to have the clue to build a relevant and efficient clinical development plan.. Very good opinion of content, presentation and speaker.”

Pierrick BOLON, R&D Clinical Manager, Boehringer Ingelheim

“Excellent. Hoped to achieve better understanding of clinical and quality parts of the dossier and this was very well accomplished. ”

Päivi Jutila, Regulatory Affairs Manager, Vetcare Ltd

“Very content with the course! The length of each chapter was nicely timed, breaks were ideal. The case we studied was a very good way to summarize all the information [seen] and it generated a lot of interesting questions/dilemmas. I would recommend.”

Emma Vanmechelen, Regulatory Affairs Specialist, DeLaval

“The content was very thorough, the presentations were held in an encouraging way and the speakers had impressive knowledge of their area and were very helpful. All [their].presentations were very valuable.”

Bernadett Riszne Ladanyi, QA Specialist/Auditor, Ceva-Phylaxia

“I enjoyed it and learned a lot. The slides are very useful reference material for later.. Nothing too lengthy so everyone could stay very focused. All speakers are very pleasant, friendly and approachable. All parts were very interesting and relevant. Mission was accomplished!”

Yannique Jacobs-Renac, Projectleader, Royal GD

“Very good general training well documented. Overall, all Very good.”

Claire Biener-Milard , RA manager, Boehringer Ingelheim