Management Forum courses now available at IPI Academy - visit IPI for an updated experience and a broader selection of courses and subjects

Training courses & Webinars:
Animal Health

The animal health industry is a growing and constantly changing market as the result of new opportunities, legislation and regulation in veterinary medicines, vaccines and feed additives. To be competitive in this field it is essential to keep up-to-date with the global requirements and have access to experts who interpret these requirements and provide practical advice on application.

Management Forum provides a wide range of animal health training courses that will give you access to leading experts and latest information within this field.

 

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

17-18 Mar 2022 - Online webinar
Also on: 6 Sep 2022

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 Tamsin Dawson (bio)
Mel Munro (bio)

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Advanced Veterinary Pharmacovigilance Training Course

Advanced Veterinary Pharmacovigilance

4-5 May 2022 - Online webinar
Also on: 21 Nov 2022

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 Apr 2022 - Online webinar
Also on: 5 Jul 2022

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

28-29 Apr 2022 - Online webinar
Also on: 30 Jun 2022

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.

Registration of Animal Feed Additives in the EU (European Union) Training Course

Registration of Animal Feed Additives in the EU

20-21 Jun 2022 - Online webinar

This course will take participants through all of the necessary steps to obtain marketing authorisation for a feed additive in the European Union.

Presented by Elinor McCartney (bio)

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The New EU (European Union) Animal Health Legislation for Veterinary Medicinal Products Training Course

The New EU Animal Health Legislation for Veterinary Medicinal Products

16-17 May 2022 - Online webinar
Also on: 3 Nov 2022

The programme will offer a comprehensive introduction to the new EU Regulation (2019/6) and will address the changes and implications to the industry including marketing authorisations, submissions and dossiers.

Presented by Julian Braidwood (bio)

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

Veterinary Pharmaceutical Submissions in the EU

9-10 Jun 2022 - Online webinar
Also on: 13 Dec 2022

Presentations will cover the regulatory framework, pharmaceutical, toxicological and pharmacological data, safety risk assessments, pre-clinical and clinical data, detailed and critical summaries and regulatory submissions.

Working Through Veterinary Drug Development in the EU (European Union) and USA Training Course

Working Through Veterinary Drug Development in the EU and USA

20-24 Jun 2022 - Online webinar
Also on: 5 Dec 2022

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

Presented by David Petrick (bio)

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[Particularly liked]: The speaker and his ability to share the information.
The complex structure of the course.
The workshop prepared for us

Daniel Pepa, Jr. Manager GRA Pharma Vetcare, B. Braun Melsungen AG

Excellent content. Knowledgeable experienced speakers. Lots of practical examples.

David Pickard, Regulatory Manager, Inroads International Ltd

Much more information was provided than I expected, it was VERY useful and well prepared.

Annette Spielbauer, Inoculant Registration and QC Associate, CORTEVA

Very clear and comprehensive presentations.

Kalinka Grozeva, Quality Control Director, Vetagro S.p.A.

The course covered all the areas I needed but it was the practical experience shared by the speaker that provided most valuable both in relation to engagement and understanding of the content...was filled with relevant, current experience between companies and regulators.

Serenia Horgan, Head of Quality Assurance, TriviumVet

I really thought Julian was excellent, very engaging, and really informed

Siobhan Crowe, Pharmacist, Univet Ltd

I enjoyed the event and even through a virtual platform it was very personable. Overall very happy with the large volume of information provided. My aspirations from the meeting were met as I wanted an overall understanding of the regulations.

Brendan Moran, Technical Director, Hygeia

during the seminar it was very clear that all speakers have a lot of experience in their fields and I liked the examples, to better understand the process and the time lines

Melanie Wergin, Medical Research Manager, Biologisce Heilmittel Heel GmbH

Very good: professional & very relevant. Also the many examples given by Elinor were really interesting

Isabelle Lardon, Regulatory affairs Coordinator, INVE

Best you can get from a webinar. Speaker as well tried to motivate the audience to give input, does not always work but thats not up to speaker.

Eva-Maria Karg, Regulatory Affairs Specialist, Boehringer Ingelheim RCV GmbH & Co KG