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. 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.

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

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 £800 per attendee
Delivery: collaborative classroom

More @ IPI Academy

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 £800 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)

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.

*INCLUDES: Interactive workshop and discussion sessions*

Rated by attendees to the public programme

Typically presented by Declan O'Rourke (bio)

Typical duration: 2 days
Pricing from £800 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 £800 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)

Delivery: collaborative classroom

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

In-house & bespoke training

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

Rated by attendees to the public programme

Typically presented by Andrew Hewitt (bio) , David Petrick (bio)

Typical duration: 5 days
Pricing from £1,500 per attendee
Delivery: collaborative classroom

More @ IPI Academy

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 £800 per attendee
Delivery: collaborative classroom

More @ IPI Academy

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...

“Content was great.
Presentation and speakers kept me engaged, so very good too. The Interactive Workshop on Product Development was a very helpful exercise”

Lillian Sibanda, Assistant Director, Australian Pesticides And Veterinary Medicines Authority

“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

“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

“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

“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 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