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
18 Mar 2024 - Online webinar
Also on: 5 Nov 2024
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.
A Practical Approach to Veterinary Vaccine Development and Registration in the EU (European Union) Training Course
11-12 Mar 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.
A Regulatory Update on Animal Feed and Feed Additives in the EU (European Union), USA and China Training Course
4-5 Dec 2023 - Online webinar
Annual two-day regulatory update on animal feed and feed additives in the EU, USA and China
Advanced Veterinary Pharmacovigilance Training Course
Introduction to Veterinary Pharmacovigilance Training Course
5-8 Feb 2024 - Online webinar
Also on: 27 Jun 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*
Practical Implementation of GCP (Good Clinical Practice) in Veterinary Field Studies Training Course
19-20 Mar 2024 - Online webinar
Also on: 26 Nov 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.
Registration of Veterinary Vaccines in the USA and Canada Training Course
17-18 Jan 2024 - Online webinar
Also on: 1 May 2024
This course will cover some of the most complex yet fundamental aspects of veterinary vaccines licensing by USDA and CFIA including the phased submission process as well as the format and content specifications for the required dossier components.
The Animal Health Summer School: Working Through Veterinary Drug Development in the EU (European Union) and USA Training Course
17-20 Jun 2024 - London
This practical four-day course provides a comprehensive understanding of veterinary medicine development in the EU and USA.
Veterinary Pharmaceutical Submissions in the EU (European Union) Training Course
12-13 Dec 2023 - London
Also on: 4 Mar 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.